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1.
Leukemia ; 17(3): 481-7, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12646934

ABSTRACT

Imatinib mesylate, an Abl-specific kinase inhibitor, produces sustained complete hematologic responses (CHR) and major cytogenetic responses (MCR) in chronic myeloid leukemia (CML) patients, but long-term outcomes in these patients are not yet known. This article reports the identification of clonal abnormalities in cells lacking detectable Philadelphia (Ph) chromosome/BCR-ABL rearrangements from seven patients with chronic- or accelerated-phase CML, who were treated with imatinib. All seven patients were refractory or intolerant to interferon therapy. Six of seven patients demonstrated MCR and one patient, who had a cryptic translocation, achieved low-level positivity (2.5%) for BCR-ABL by fluorescence in situ hybridization. The median duration of imatinib treatment before the identification of cytogenetic abnormalities in BCR-ABL-negative cells was 13 months. The most common cytogenetic abnormality was trisomy 8, documented in three patients. All patients had varying degrees of dysplastic morphologic abnormalities. One patient exhibited increased numbers of marrow blasts, yet consistently demonstrated no Ph-positive metaphases and the absence of morphologic features of CML. The presence of clonal abnormalities in Ph-negative cells of imatinib-treated CML patients with MCR and CHR highlights the importance of routine metaphase cytogenetic testing and long-term follow-up of all imatinib-treated patients.


Subject(s)
Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy , Neoplasm, Residual/genetics , Philadelphia Chromosome , Piperazines/pharmacology , Pyrimidines/pharmacology , Adult , Aged , Benzamides , Case-Control Studies , Chromosomes, Human, Pair 8 , Clone Cells/drug effects , Clone Cells/metabolism , Clone Cells/pathology , Cytogenetic Analysis , Female , Follow-Up Studies , Humans , Imatinib Mesylate , Leukemia, Myelogenous, Chronic, BCR-ABL Positive/pathology , Male , Middle Aged , Neoplasm, Residual/pathology , Piperazines/administration & dosage , Piperazines/therapeutic use , Pyrimidines/administration & dosage , Pyrimidines/therapeutic use , Reverse Transcriptase Polymerase Chain Reaction , Trisomy
2.
Genes Chromosomes Cancer ; 32(4): 342-52, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11746975

ABSTRACT

Studies examining altered imprinted gene expression in cancer compare the observed expression pattern to the normal expression pattern for a given tissue of origin, usually the somatic expression pattern for the imprinted gene. Germ cell tumors (GCTs), however, require a developmental stage-dependent comparison. To explore using methylation as an indicator of germ cell development, we determined the pattern of methylation at the 5' untranslated region of SNRPN in 89 GCTs from both children and adults. Fifty-one of 84 tumors (60.7%) (12/30 (40%) of cultured pediatric GCTs, 23/36 (63.9%) of frozen adult GCTs, and 16/23 (69.5%) of frozen pediatric GCTs, with five samples having results from both cultured and uncultured material) demonstrated a nonsomatic methylation pattern after dual digestion with XbaI, NotI, and Southern blot analysis. In contrast, only 2 of 18 (11%) control samples (16 non-GCTs and 2 normal ovaries) exhibited a nonsomatic pattern. In both cases, the result was shown to be due to copy number differences between maternal and paternal homologs, unlike the GCTs in which there was no evidence of an uneven homolog number. A comparison of the data for only the gonadal GCTs and the control data showed a highly significant difference in the proportion of tumors with methylation alterations at this locus (P = 0.0000539). Since there is no published evidence of the involvement of SNRPN methylation changes in the development of malignancy, the data suggest that the methylation pattern of SNRPN in GCTs reflects that of the primordial germ cell giving rise to the tumor.


Subject(s)
Autoantigens/genetics , DNA Methylation , Germ Cells/growth & development , Germinoma/genetics , Germinoma/pathology , Adolescent , Adult , Child , Child, Preschool , DNA, Neoplasm/metabolism , Female , Genomic Imprinting/genetics , Germ Cells/pathology , Germinoma/metabolism , Germinoma/secondary , Humans , Infant , Infant, Newborn , Male , Ribonucleoproteins, Small Nuclear/genetics , Tumor Cells, Cultured , snRNP Core Proteins
3.
Mol Pharmacol ; 60(6): 1181-8, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11723224

ABSTRACT

The trace amine para-tyramine is structurally and functionally related to the amphetamines and the biogenic amine neurotransmitters. It is currently thought that the biological activities elicited by trace amines such as p-tyramine and the psychostimulant amphetamines are manifestations of their ability to inhibit the clearance of extracellular transmitter and/or stimulate the efflux of transmitter from intracellular stores. Here we report the discovery and pharmacological characterization of a rat G protein-coupled receptor that stimulates the production of cAMP when exposed to the trace amines p-tyramine, beta-phenethylamine, tryptamine, and octopamine. An extensive pharmacological survey revealed that psychostimulant and hallucinogenic amphetamines, numerous ergoline derivatives, adrenergic ligands, and 3-methylated metabolites of the catecholamine neurotransmitters are also good agonists at the rat trace amine receptor 1 (rTAR1). These results suggest that the trace amines and catecholamine metabolites may serve as the endogenous ligands of a novel intercellular signaling system found widely throughout the vertebrate brain and periphery. Furthermore, the discovery that amphetamines, including 3,4-methylenedioxymethamphetamine (MDMA; "ecstasy"), are potent rTAR1 agonists suggests that the effects of these widely used drugs may be mediated in part by this receptor as well as their previously characterized targets, the neurotransmitter transporter proteins.


Subject(s)
Amphetamine/pharmacology , Lysergic Acid Diethylamide/pharmacology , N-Methyl-3,4-methylenedioxyamphetamine/pharmacology , Receptors, Biogenic Amine/agonists , Amino Acid Sequence , Animals , Catecholamines/metabolism , Catecholamines/pharmacology , Chromosome Mapping , Chromosomes, Human, Pair 6 , Cloning, Molecular , Dopamine Agents/pharmacology , Humans , Molecular Sequence Data , Neurotransmitter Agents/pharmacology , Rats , Receptors, Biogenic Amine/metabolism , Sequence Homology, Amino Acid , Serotonin Agents/pharmacology , Subcellular Fractions , Tumor Cells, Cultured
4.
Am J Med Genet ; 101(2): 100-5, 2001 Jun 15.
Article in English | MEDLINE | ID: mdl-11391651

ABSTRACT

Interstitial duplications of chromosomes 1p are rare, with only 14 cases previously reported in the literature, and those have not revealed a unique syndrome. The phenotypes include multiple congenital abnormalities and both intra- and extra-uterine growth retardation. In general, the patients do poorly and do not survive beyond the age of several months. We report a newborn male with karyotype 46, XY, inv dup(1)(qter--> p34.3::p34.3-->p32.3::34.3-->pter) with multiple congenital abnormalities including congenital heart disease and co-existing portal and pulmonary hypertension. The chromosome 1 origin of the extra material was confirmed with fluorescent in situ hybridization (FISH). Review of the GDB [Human Genome Database, 1990] reveals that the duplicated region includes the locus EDN2 that encodes endothelin-1, a potent vasoconstrictor, making genetic overdosage of this protein a likely etiology of the pulmonary hypertension. The diffuse abnormalities show effects in multiple cell lines and suggest that this region of chromosome 1p could be involved in determining cell migration and/or differentiation during organogenesis.


Subject(s)
Abnormalities, Multiple/genetics , Chromosome Aberrations , Chromosomes, Human, Pair 1/genetics , Heart Defects, Congenital/genetics , Abnormalities, Multiple/pathology , Chromosome Banding , Fatal Outcome , Gene Duplication , Heart Defects, Congenital/pathology , Humans , In Situ Hybridization, Fluorescence , Infant , Infant, Newborn , Male
5.
Cancer Genet Cytogenet ; 125(2): 112-8, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11369053

ABSTRACT

Chromosome studies of pediatric germ cell tumors (GCTs) show differences in abnormalities dependent on age, sex, tumor location, and histology. Previous studies suggest that loss of 1p is associated with a malignant phenotype, while amplification of 12p, a common finding in adult testicular GCTs, is uncommon in pediatric GCTs. Fifty-three pediatric GCTs were analyzed for 1p36 loss and 12p amplification by G-banding and dual-color interphase FISH with probes for the centromere and short arm of chromosomes 1 or 12. Twelve tumors with loss of 1p36 were identified. No deletion was detected in tumors with nonmalignant histology, such that there was a significant association of 1p loss with malignancy in these tumors (P = 0.00115). Five of 18 tumors from male patients had amplification of 12p, consistent with G-band results. Combined analysis of our data with those in the literature revealed a significant correlation of 12p amplification with patient age (P = 0.000196). Amplification of 12p was only seen in one of 35 tumors from female patients. Five female GCTs had numerical abnormalities of chromosome 12, and two tumors showed complete lack of 12p. This spectrum of abnormalities differs from what is seen in the male tumors, providing further evidence for different etiologies of GCTs between the sexes.


Subject(s)
Chromosome Aberrations , Chromosomes, Human, Pair 12/ultrastructure , Chromosomes, Human, Pair 1/ultrastructure , Germinoma/genetics , In Situ Hybridization, Fluorescence , Adolescent , Aneuploidy , Child , Child, Preschool , Chromosome Deletion , Female , Gene Amplification , Germinoma/pathology , Humans , Infant , Infant, Newborn , Interphase , Male , Sex Factors
6.
Am J Med Genet ; 99(3): 210-6, 2001 Mar 15.
Article in English | MEDLINE | ID: mdl-11241492

ABSTRACT

The prenatal diagnosis of trisomy 20 mosaicism presents a challenge for practitioners and parents. The diagnosis implies an uncertain risk for an inconsistent set of physical and developmental findings, as well as a substantial chance for a child that is normal physically and developmentally. We report two girls (ages nine years one month and eight years one month) with normal intelligence and hypopigmented skin areas. Both girls were born after a prenatal diagnosis of trisomy 20 mosaicism in amniocytes. Case 1 had 83% and 57% trisomy 20 cells from two separate amniocenteses and Case 2 had 90% trisomy 20 cells from an amniocentesis. Trisomy 20 was confirmed after birth in urinary sediment (25%) and chorionic villus cells (15%) in Case 1, while cord blood lymphocytes (30 cells) and skin fibroblasts (50 cells) had only 46,XX cells. Trisomy 20 was confirmed after birth in urinary sediment (100%), placenta (100%), cord (10%), amniotic membrane (50%), and skin fibroblasts (30%) in Case 2, while cord blood lymphocytes (100 cells) had only 46,XX cells. This is the first report of a hypopigmented pigmentary dysplasia associated with isolated trisomy 20 mosaicism. Our patients are the oldest reported children with trisomy 20 mosaicism confirmed after birth.


Subject(s)
Chromosomes, Human, Pair 20 , Hypopigmentation/genetics , Intelligence/genetics , Mosaicism , Trisomy/genetics , Female , Humans , Hypopigmentation/diagnosis , Infant, Newborn , Prenatal Diagnosis , Trisomy/diagnosis
7.
Genes Chromosomes Cancer ; 25(2): 134-46, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10337997

ABSTRACT

The chromosomes of 81 pediatric germ cell tumors (GCTs) were analyzed as part of two clinical treatment trials, INT-0098 and INT-0097, conducted by the Children's Cancer Group. The analysis of chromosome results showed differences with respect to sex, age, tumor location, and histology. Sixteen of 17 benign teratomas of infants and children less than 4 years old and from gonadal and extragonadal locations were chromosomally normal. Twenty-three malignant GCTs from gonadal and extragonadal locations of the same age group were endodermal sinus tumors and varied in their karyotypic findings. The most common abnormalities were gains of 1q and chromosome 3. Of eight benign ovarian teratomas from older girls, five with normal G-banded karyotypes were determined to be homozygous for Q-band heteromorphisms, suggesting a meiosis II error. Among the 12 malignant ovarian GCTs from older girls, the common abnormalities were loss of 1p/gain of 1q, +3, +8, +14, and +21. Four of eight extragonadal tumors from older boys demonstrated +21; one had +X. Five of the eight had associated constitutional chromosome abnormalities, including one trisomy 21 and three with Klinefelter syndrome. The testicular GCTs of adolescents had abnormalities resembling those found in adult testicular GCT, including near-triploidy, loss of chromosomes 11, 13, and 18, and gain of chromosomes 7, 8, the X chromosome, and an isochromosome 12p. The gain of an isochromosome 12p was only frequent in the tumors from adolescent boys. Deletion of 1p/gain of 1q and +3 were the most common abnormalities among the malignant tumors from both sexes.


Subject(s)
Chromosome Aberrations/genetics , Neoplasms, Germ Cell and Embryonal/genetics , Abdominal Neoplasms/genetics , Abdominal Neoplasms/pathology , Adolescent , Adult , Age Factors , Bone Neoplasms/genetics , Bone Neoplasms/pathology , Child , Child, Preschool , Chromosome Aberrations/pathology , Chromosome Disorders , Chromosomes, Human, Pair 18/genetics , Clinical Trials as Topic , Female , Humans , Infant , Infant, Newborn , Karyotyping , Male , Neoplasms, Germ Cell and Embryonal/pathology , Ovarian Neoplasms/genetics , Ovarian Neoplasms/pathology , Ploidies , Sacrococcygeal Region/pathology , Sex Factors , Testicular Neoplasms/genetics , Testicular Neoplasms/pathology
8.
Am J Med Genet ; 78(1): 36-43, 1998 Jun 16.
Article in English | MEDLINE | ID: mdl-9637421

ABSTRACT

We present clinical outcome, through several years of follow-up, of 4 mentally retarded patients, each with a small interstitial deletion in the long arm of chromosome 2, within a region on which clinical reports are infrequent. Our patient 1 was found to have del(2)(q22.3q23.3); patients 2 and 3, del(2)(q23.3q24.2); and patient 4, del(2) (q24.2q31). By comparison of our cases with each other and with those previously published with comparable interstitial deletion, we attempted to identify characteristic clinical findings. Short neck with excessive cervical skin was seen with monosomy of chromosome 2 bands q22.3-q23.3, while hypertrichosis and a peculiar high pitched cry were seen with monosomy of chromosome 2 bands q23.3-q24.2. As suggested by Moller et al. [1984: Hum Genet 68:77-86], a cleft between the first and second toes was seen with monosomy of chromosome 2 bands q24.2-q31. In addition, seizure disorder was present in patients 1 and 4 (with the more proximal and distal deletions, respectively).


Subject(s)
Chromosome Aberrations/genetics , Chromosome Deletion , Chromosomes, Human, Pair 2 , Adult , Child , Chromosome Disorders , Female , Follow-Up Studies , Humans , Intellectual Disability/genetics , Male , Seizures/genetics
9.
Blood ; 91(1): 275-87, 1998 Jan 01.
Article in English | MEDLINE | ID: mdl-9414295

ABSTRACT

Cells from individuals with Fanconi anemia (FA) arrest excessively in the G2/M cell cycle compartment after exposure to low doses of DNA cross-linking agents. The relationship of this abnormality to the fundamental genetic defect in such cells is unknown, but many investigators have speculated that the various FA genes directly regulate cell cycle checkpoints. We tested the hypothesis that the protein encoded by the FA group C complementing gene (FAC) functions to control a cell cycle checkpoint and that cells from group C patients (FA[C]) have abnormalities of cell cycle regulation directly related to the genetic mutation. We found that retroviral transduction of FA(C) lymphoblasts with wild-type FAC cDNA resulted in normalization of the cell cycle response to low-dose mitomycin C (MMC). However, when DNA damage was quantified in terms of cytogenetic damage or cellular cytotoxicity, we found similar degrees of G2/M arrest in response to equitoxic amounts of MMC in FA(C) cells as well as in normal lymphoblasts. Similar results were obtained using isogenic pairs of uncorrected, FAC- or mock-corrected (neo only) FA(C) cell lines. To test the function of other checkpoints we examined the effects of hydroxyurea (HU) and ionizing radiation on cell cycle kinetics of FA(C) and normal lymphoblasts as well as with isogenic pairs of uncorrected, FAC-corrected, or mock-corrected FA(C) cell lines. In all cases the cell cycle response of FA(C) and normal lymphoblasts to these two agents were identical. Based on these studies we conclude that the aberrant G2/M arrest that typifies the response of FA(C) cells to low doses of cross-linking agents does not represent an abnormal cell cycle response but instead represents a normal cellular response to the excessive DNA damage that results in FA(C) cells following exposure to low doses of cross-linking agents.


Subject(s)
Caffeine/pharmacology , Cross-Linking Reagents/pharmacology , DNA Damage/drug effects , DNA/drug effects , Fanconi Anemia/pathology , G2 Phase/drug effects , Hydroxyurea/pharmacology , Lymphocytes/drug effects , Metaphase/drug effects , Mitomycin/pharmacology , Cell Line, Transformed , DNA/radiation effects , DNA Damage/radiation effects , DNA, Complementary/genetics , Fanconi Anemia/genetics , G2 Phase/radiation effects , Humans , Lymphocytes/pathology , Lymphocytes/radiation effects , Metaphase/radiation effects , Transfection
10.
Cytogenet Cell Genet ; 79(3-4): 276-81, 1997.
Article in English | MEDLINE | ID: mdl-9605871

ABSTRACT

Smith-Magenis syndrome (SMS) comprises a complex physical and behavioral phenotype that is associated with an interstitial deletion of chromosome 17p11.2. The deletions observed in patients can range from <2 to >9 megabases of DNA and may include more than 100 genes. In order to determine the critical deletion interval responsible for the syndrome phenotype, we have examined several patients with varying deletions involving 17p11.2 by somatic cell hybrid analyses. We have binned 112 markers along 17p11.2, including 27 markers within the critical interval for SMS, which is bound proximally by D17S29 and distally by cCI17-638. In addition, we present two patients who carry deletions involving 17p11.2 but do not exhibit the typical features of SMS. Patients such as these will allow genotype:phenotype correlations to be made and the gene(s) responsible for the SMS phenotype to be determined.


Subject(s)
Abnormalities, Multiple/genetics , Chromosome Deletion , Chromosomes, Human, Pair 17 , Adolescent , Child, Preschool , Genetic Markers , Humans , Hybrid Cells , Syndrome
11.
Am J Med Genet ; 66(1): 25-7, 1996 Dec 02.
Article in English | MEDLINE | ID: mdl-8957506

ABSTRACT

Recently we reported on three unrelated children with neural tube defects (NTDs) and deletion of 22q11. Two of these children have velo-cardio-facial syndrome and the third DiGeorge sequence. Thus, NTDs appear to be part of the clinical picture due to 22q11 deletion. To further explore this association and to clarify what findings should prompt testing for this deletion in individuals with NTDs, we have reviewed all patients in a large regional spina bifida clinic population. Two hundred ninety-five patients with NTDs were identified by chart review. Charts were reviewed for congenital heart defect, minor facial anomalies, thymic hypoplasia, cleft lip and/or palate, hypocalcemia, and a family history of a NTD, congenital heart defect, or cleft lip and/or palate. A total of 22 patients was identified with NTD and at least one more clinical trait and/or a positive family history. Sixteen children received cytogenetic and molecular testing including the three previously reported patients diagnosed with a 22q11 deletion. Results of cytogenetic and molecular studies of the remaining 13 patients were normal. Deletion of 22q11 is an infrequent cause of NTDs. We recommend testing for the 22q11 deletion in patients with a NTD and conotruncal heart defect. Testing should be considered in patients with a NTD who have a first degree relative with a conotruncal heart defect or have additional clinical findings of VCFS or DGS.


Subject(s)
Chromosome Deletion , Chromosomes, Human, Pair 22 , Neural Tube Defects/genetics , Child , DiGeorge Syndrome/genetics , Genetic Markers , Heart Defects, Congenital/genetics , Humans
12.
Cancer Genet Cytogenet ; 92(2): 116-21, 1996 Dec.
Article in English | MEDLINE | ID: mdl-8976367

ABSTRACT

We describe a malignant epithelioid hemangioendothelioma arising in the back of a 45-year-old man with pulmonary and bone marrow metastases. Light microscopic and immunohistochemical features of this tumor are presented. Karyotyping revealed several clonal abnormalities: a complex unbalanced translocation [7;22] involving multiple breakpoints (confirmed by fluorescence in situ hybridization), a Robertsonian t(14;14), and loss of the Y chromosome. Monosomy for chromosome 11 was noted in a subset of the tumor cells. To our knowledge a karyotype has not been previously reported for this unusual vascular tumor.


Subject(s)
Chromosomes, Human, Pair 22 , Chromosomes, Human, Pair 7 , Hemangioendothelioma, Epithelioid/genetics , Hemangioendothelioma, Epithelioid/pathology , Muscle Neoplasms/genetics , Muscle Neoplasms/pathology , Translocation, Genetic , Bone Neoplasms/secondary , Chromosome Banding , Chromosome Mapping , Hemangioendothelioma, Epithelioid/secondary , Hemangioendothelioma, Epithelioid/surgery , Humans , Karyotyping , Lung Neoplasms/secondary , Male , Middle Aged , Muscle Neoplasms/surgery
13.
Am J Hum Genet ; 58(5): 1008-16, 1996 May.
Article in English | MEDLINE | ID: mdl-8651261

ABSTRACT

Prader-Willi syndrome (PWS) is most often the result of a deletion of bands q11.2-q13 of the paternally derived chromosome 15, but it also occurs either because of maternal uniparental disomy (UPD) of this region or, rarely, from a methylation imprinting defect. A significant number of cases are due to structural rearrangements of the pericentromeric region of chromosome 15. We report two cases of PWS with UPD in which there was a meiosis I nondisjunction error involving an altered chromosome 15 produced by both a translocation event between the heteromorphic satellite regions of chromosomes 14 and 15 and recombination. In both cases, high-resolution banding of the long arm was normal, and FISH of probes D15S11, SNRPN, D15S10, and GABRB3 indicated no loss of this material. Chromosome heteromorphism analysis showed that each patient had maternal heterodisomy of the chromosome 15 short arm, whereas PCR of microsatellites demonstrated allele-specific maternal isodisomy and heterodisomy of the long arm. SNRPN gene methylation analysis revealed only a maternal imprint in both patients. We suggest that the chromosome structural rearrangements, combined with recombination in these patients, disrupted normal segregation of an imprinted region, resulting in uniparental disomy and PWS.


Subject(s)
Chromosomes, Human, Pair 14 , Chromosomes, Human, Pair 15 , Genomic Imprinting , Prader-Willi Syndrome/genetics , Adult , Child , Chromosome Banding , Female , Humans , Male , Polymorphism, Genetic , Recombination, Genetic , Translocation, Genetic
14.
Hum Genet ; 97(5): 642-9, 1996 May.
Article in English | MEDLINE | ID: mdl-8655146

ABSTRACT

Autosomal dominant Charcot-Marie-Tooth type-1A neuropathy (CMT1A) is a demyelinating peripheral nerve disorder that is commonly associated with a submicroscopic tandem DNA duplication of a 1.5-Mb region of 17p11.2p12 that contains the peripheral myelin gene PMP22. Clinical features of CMT1A include progressive distal muscle atrophy and weakness, foot and hand deformities, gait abnormalities, absent reflexes, and the completely penetrant electrophysiologic phenotype of symmetric reductions in motor nerve conduction velocities (NCVs). Molecular and fluorescense in situ hybridization (FISH) analyses were performed to determine the duplication status of the PMP22 gene in four patients with rare cytogenetic duplications of 17p. Neuropathologic features of CMT1A were seen in two of these four patients, in addition to the complex phenotype asociated with 17p partial trisomy. Our findings show that the CMT1A phenotype of reduced NCV is specifically associated with PMP22 gene duplications, thus providing further support for the PMP22 gene dosage mechanism for CMT1A.


Subject(s)
Charcot-Marie-Tooth Disease/genetics , Chromosomes, Human, Pair 17 , Multigene Family , Myelin Proteins/genetics , Trisomy , Blotting, Southern , Charcot-Marie-Tooth Disease/pathology , Charcot-Marie-Tooth Disease/physiopathology , Child, Preschool , Chromosome Banding , Chromosome Mapping , Electrophysiology , Female , Genes, Dominant , Humans , In Situ Hybridization, Fluorescence , Male , Motor Neurons/physiology , Neural Conduction , Pedigree , Phenotype , Sural Nerve/physiopathology
15.
Am J Med Genet ; 57(4): 588-97, 1995 Jul 17.
Article in English | MEDLINE | ID: mdl-7573135

ABSTRACT

Interstitial deletions of chromosome 4 have been described rarely and have had variable presentations. We describe the phenotypic characteristics associated with interstitial deletion of the p14-16 region of chromosome 4 in 7 patients with multiple minor anomalies in common, and with mental retardation. A review of published cases of interstitial deletions of the short arm of chromosome 4 is provided. These deletions present a distinct phenotype which is different from that of Wolf-Hirschhorn syndrome.


Subject(s)
Abnormalities, Multiple/genetics , Chromosome Deletion , Chromosomes, Human, Pair 4 , Intellectual Disability/genetics , Abnormalities, Multiple/pathology , Adult , Aged , Chromosome Mapping , Female , Humans , Infant , Intellectual Disability/pathology , Karyotyping , Male , Pedigree , Phenotype
16.
Br J Haematol ; 90(2): 266-73, 1995 Jun.
Article in English | MEDLINE | ID: mdl-7794746

ABSTRACT

The clinicopathological features and the prognostic significance of acute myeloid leukaemia (AML) with trisomy 11 are currently unknown. In this study we describe 15 adult AML cases with trisomy 11. Trisomy 11 was the sole chromosomal anomaly in eight cases; the remaining seven cases were characterized by +11 in association with other karyotypic aberrations. Patients ages ranged from 34 to 79 years. 12 patients were male; three were female. Although there was no correlation of trisomy 11 with any specific FAB subgroup [M2 (n = 7), M1 (n = 5), M4/5 (n = 2), M3 (n = 1)] less mature forms predominated. Immunologically, the leukaemic blasts showed a strikingly consistent stem cell phenotype with expression of HLA-DR, CD34 and the myeloid antigens (CD15, CD33 and/or CD13). In addition, two cases expressed the B-cell associated antigen CD19. The presence of trilineage dysplasia, suggesting the presence of an underlying myelodysplasia (MDS), was observed at presentation in five cases; in another case MDS was evident at relapse only. Unexpectedly, MLL gene rearrangements were observed in two of four cases characterized by trisomy 11 as the sole karyotypic abnormality; however, MLL aberrations were not identified in three cases with trisomy 11 accompanied by other karyotypic anomalies. The majority of patients in each subgroup (i.e. those with and without additional cytogenetic abnormalities) achieved a short first complete remission (CR) (mean 8 months) and failed to obtain a second CR. Only one patient in each trisomy 11 subgroup is in a continuous CR for > 34 months. These findings suggest that trisomy 11 leukaemia is characterized by a stem/progenitor cell immunophenotype with poor response to standard chemotherapeutic regimens and an unfavourable prognosis.


Subject(s)
Chromosomes, Human, Pair 11 , Leukemia, Myeloid/genetics , Trisomy , Acute Disease , Adult , Aged , Blotting, Southern , Female , Humans , Immunophenotyping , Karyotyping , Leukemia, Myeloid/immunology , Leukemia, Myeloid/pathology , Male , Middle Aged , Mutation , Myelodysplastic Syndromes/complications , Myelodysplastic Syndromes/immunology , Myelodysplastic Syndromes/pathology , Treatment Outcome
17.
Am J Hum Genet ; 56(5): 1042-51, 1995 May.
Article in English | MEDLINE | ID: mdl-7726157

ABSTRACT

Fragile X syndrome is the most common form of inherited mental retardation and results from the transcriptional inactivation of the FMR1 gene. In the vast majority of cases, this is caused by the expansion of an unstable CGG repeat in the first exon of the FMR1 gene. We describe here a phenotypically atypical case of fragile X syndrome, caused by a deletion that includes the entire FMR1 gene and > or = 9.0 Mb of flanking DNA. The proband, RK, was a 6-year-old mentally retarded male with obesity and anal atresia. A diagnosis of fragile X syndrome was established by the failure of RK's DNA to hybridize to a 558-bp PstI-XhoI fragment (pfxa3) specific for the 5'-end of the FMR1 gene. The analysis of flanking markers in the interval from Xq26.3-q28 indicated a deletion extending from between 160-500 kb distal and 9.0 Mb proximal to the FMR1 gene. High-resolution chromosome banding confirmed a deletion with breakpoints in Xq26.3 and Xq27.3. This deletion was maternally transmitted and arose as a new mutation on the grandpaternal X chromosome. The maternal transmission of the deletion was confirmed by FISH using a 34-kb cosmid (c31.4) containing most of the FMR1 gene. These results indicated that RK carried a deletion of the FMR1 region with the most proximal breakpoint described to date. This patient's unusual clinical presentation may indicate the presence of genes located in the deleted interval proximal to the FMR1 locus that are able to modify the fragile X syndrome phenotype.


Subject(s)
Fragile X Syndrome/genetics , Gene Deletion , Nerve Tissue Proteins/genetics , RNA-Binding Proteins , Adult , Blotting, Southern , Child, Preschool , Chromosome Banding , DNA/chemistry , Female , Fragile X Mental Retardation Protein , Humans , In Situ Hybridization, Fluorescence , Karyotyping , Male , Methylation , Pedigree
19.
Am J Med Genet ; 55(4): 444-52, 1995 Feb 13.
Article in English | MEDLINE | ID: mdl-7762584

ABSTRACT

With improvements in culturing and banding techniques, amniotic fluid studies now achieve a level of resolution at which the Prader-Willi syndrome (PWS) and Angelman syndrome (AS) region may be questioned. Chromosome 15 heteromorphisms, detected with Q- and R-banding and used in conjunction with PWS/AS region-specific probes, can confirm a chromosome deletion and establish origin to predict the clinical outcome. We report four de novo cases of an abnormal-appearing chromosome 15 in amniotic fluid samples referred for advanced maternal age or a history of a previous chromosomally abnormal child. The chromosomes were characterized using G-, Q-, and R-banding, as well as isotopic and fluorescent in situ hybridization of DNA probes specific for the proximal chromosome 15 long arm. In two cases, one chromosome 15 homolog showed a consistent deletion of the ONCOR PWS/AS region A and B. In the other two cases, one of which involved an inversion with one breakpoint in the PWS/AS region, all of the proximal chromosome 15 long arm DNA probes used in the in situ hybridization were present on both homologs. Clinical follow-up was not available on these samples, as in all cases the parents chose to terminate the pregnancies. These cases demonstrate the ability to prenatally diagnose chromosome 15 abnormalities associated with PWS/AS. In addition, they highlight the need for a better understanding of this region for accurate prenatal diagnosis.


Subject(s)
Angelman Syndrome/diagnosis , Angelman Syndrome/genetics , Chromosome Deletion , Chromosomes, Human, Pair 15 , Prader-Willi Syndrome/diagnosis , Prader-Willi Syndrome/genetics , Prenatal Diagnosis , Adult , Chromosome Banding , DNA Probes , Female , Humans , In Situ Hybridization , In Situ Hybridization, Fluorescence , Male , Pregnancy
20.
Am J Med Genet ; 52(4): 445-9, 1994 Oct 01.
Article in English | MEDLINE | ID: mdl-7747757

ABSTRACT

Approximately 5% of children with neural tube defects (NTDs) have a congenital heart defect and/or cleft lip and palate. The cause of isolated meningomyelocele, congenital heart defects, or cleft lip and palate has been largely thought to be multifactorial. However, chromosomal, teratogenic, and single gene causes of combinations of NTDs with congenital heart defects and/or cleft lip and palate have been reported. We report on 3 patients with meningomyelocele, congenital heart defects, and 22q11 deletions. Two of the children had the clinical diagnosis of velo-cardio-facial syndrome (VCFS); both also have bifid uvula. The third child had DiGeorge sequence (DGS). The association of NTDs with 22q11 deletions has not been reported previously. An accurate diagnosis of the 22q11 deletion is critical as this micro-deletion and its associated clinical problems is transmitted as an autosomal dominant trait due to the inheritance of the deletion-bearing chromosome. We recommend that all children with NTDs and congenital heart defects, with or without cleft palate, have cytogenetic and molecular studies performed to detect 22q11 deletions.


Subject(s)
Chromosome Deletion , Chromosomes, Human, Pair 22/genetics , DiGeorge Syndrome/genetics , Face/abnormalities , Heart Defects, Congenital/genetics , Meningomyelocele/genetics , Adult , Blotting, Southern , Child , Child, Preschool , Cytogenetics , Family Health , Female , Humans , In Situ Hybridization, Fluorescence , Infant , Infant, Newborn , Male , Meningomyelocele/complications , Polymorphism, Restriction Fragment Length , Pregnancy
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