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1.
Am J Clin Pathol ; 142(2): 248-53, 2014 Aug.
Article in English | MEDLINE | ID: mdl-25015868

ABSTRACT

OBJECTIVES: We report here the unusual association of Silver-Russell syndrome (SRS) and cerebellar dysplasia with trisomy 7 mosaicism and maternal uniparental disomy of chromosome 7 [UPD(7)m]. METHODS: Low-level trisomy 7 mosaicism was diagnosed prenatally on amniocytes, and UPD(7)m was confirmed after birth. RESULTS: Medical examination at birth showed dysmorphic facial features of SRS. Cytogenetic analysis on several tissues and cells confirmed mosaic trisomy 7. Unusual severe psychomotor retardation, hypotonia, and choreoathetoid movement were noted at 6 months. Brain magnetic resonance imaging showed both cerebellar hypoplasia and dysplasia. CONCLUSIONS: This unusual association of SRS and dysplasia of the cerebellum might be related to the presence of the trisomy 7 mosaicism on the cerebellum. Our observation strengthens the hypothesis that the phenotype observed in patients with SRS with UPD(7)m might also result from an undetected low level of trisomy 7 mosaicism that could best be revealed by performing cytogenetic investigations.


Subject(s)
Brain/pathology , Silver-Russell Syndrome/genetics , Trisomy/genetics , Uniparental Disomy/genetics , Adult , Cerebellum/abnormalities , Chromosomes, Human, Pair 7/genetics , Cytogenetic Analysis , Developmental Disabilities/diagnosis , Female , Humans , Mosaicism , Nervous System Malformations/diagnosis , Silver-Russell Syndrome/complications , Silver-Russell Syndrome/diagnosis
2.
Am J Med Genet A ; 158A(4): 894-900, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22419357

ABSTRACT

Small supernumerary marker chromosome (sSMC) lacking alpha satellite DNA or endogenous centromere regions are rare and contain fully functional centromeres, called neocentromeres. We report on a woman with a 14-week gestation pregnancy with a cystic hygroma and cerebellar hypoplasia at ultrasound examination. Cytogenetic studies showed a karyotype 47,XY,+mar dn. This sSMC was observed in chorionic villi, lung, and muscle tissue. Array Comparative Genomic Hybridization showed a gain from 13q31.1 to 13qter region. Fluorescent in situ hybridization with pan alpha satellite probe and probes specific for chromosome 13 showed a marker corresponding to an inversion duplication of the 13q distal chromosomal region without alpha satellite DNA sequence, suggesting the presence of a neocentromere. Examination of the fetus showed dysmorphic features, cystic cervical hygroma, postaxial polydactyly of the right hand and left foot with short fingers, malrotation of the gut, and a micropenis with hypospadias. Genotype-phenotype correlation in tetrasomy 13q is discussed according to the four 13q chromosomal breakpoints reported (13q32, 13q31, 13q21, 13q14) for chromosome 13 supernumerary markers.


Subject(s)
Abnormalities, Multiple/genetics , Chromosome Inversion , Chromosomes, Human, Pair 13/genetics , Fetus/abnormalities , Tetrasomy , Cerebellum/abnormalities , Chromosome Banding , Comparative Genomic Hybridization , Female , Genetic Association Studies , Humans , In Situ Hybridization, Fluorescence , Karyotype , Lymphangioma, Cystic , Male , Pregnancy , Pregnancy Complications/genetics , Ultrasonography, Prenatal
3.
Eur J Med Genet ; 54(5): e489-94, 2011.
Article in English | MEDLINE | ID: mdl-21741501

ABSTRACT

Pure interstitial deletions of the long arm of chromosome 13 are correlated with variable phenotypes according to the size and the location of the deleted region. Deletions involving the 13q13q21 region are rare. In order to establish interstitial 13q genotype-phenotype correlation, we used high resolution 244K oligonucleotide array in addition to conventional karyotype and molecular (fluorescent in situ hybridization, microsatellite markers analysis) techniques in two independent probands carrying a deletion 13q13 to 13q21. First patient was a 3-year-old girl with mental retardation and dysmorphy carrying a 13q13.3q21.31 de novo deletion diagnosed post-natally. The second one was a fetus with de novo del(13)(q14q21.2) associated with first trimester increased nuchal translucency. We showed that specific dysmorphic features (macrocephaly, high forehead, hypertelorism, large nose, large and malformed ears and retrognathia) were correlated to the common 13q14q21 chromosomal segment. Physical examination revealed overgrowth with global measurement up to the 95th percentile in both probands. This is the second description of overgrowth in patients carrying a 13q deletion. Haploinsufficiency of common candidates genes such as CKAP2, SUGT1, LECT1, DCLK1 and SMAD9, involved in cell division and bone development, is a possible mechanism that could explain overgrowth in both patients. This study underlines also that cytogenetic analysis could be performed in patients with overgrowth.


Subject(s)
Chromosome Disorders/genetics , Genetic Association Studies , Adult , Child, Preschool , Chromosome Deletion , Chromosomes, Human, Pair 13/genetics , Comparative Genomic Hybridization , Female , Fetus , Humans , In Situ Hybridization, Fluorescence , Infant , Karyotyping , Microsatellite Repeats/genetics , Phenotype , Pregnancy , Prenatal Diagnosis , Young Adult
4.
Eur J Hum Genet ; 19(9): 959-64, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21522184

ABSTRACT

With the clinical implementation of genomic microarrays, the detection of cryptic unbalanced rearrangements in patients with syndromic developmental delay has improved considerably. Here we report the molecular karyotyping and phenotypic description of six new unrelated patients with partially overlapping microdeletions at 10p12.31p11.21 ranging from 1.0 to 10.6 Mb. The smallest region of overlap is 306 kb, which includes WAC gene, known to be associated with microtubule function and to have a role in cell division. Another patient has previously been described with a 10 Mb deletion, partially overlapping with our six patients. All seven patients have developmental delay and a majority of the patients have abnormal behaviour and dysmorphic features, including bulbous nasal tip, deep set eyes, synophrys/thick eyebrows and full cheeks, whereas other features varied. All patients also displayed various visual impairments and six out of seven patients had cardiac malformations. Taken together with the previously reported patient, our study suggests that the detected deletions may represent a new contiguous gene syndrome caused by dosage-sensitive genes that predispose to developmental delay.


Subject(s)
Chromosomes, Human, Pair 10/genetics , Developmental Disabilities/genetics , Sequence Deletion/genetics , Adolescent , Child , Child, Preschool , DNA Copy Number Variations/genetics , Female , Humans , Male , Oligonucleotide Array Sequence Analysis , Syndrome
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