Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 6 de 6
Filter
2.
Prenat Diagn ; 35(1): 81-9, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25174624

ABSTRACT

OBJECTIVE: The aim of the present study was to assess the risk of major anomalies in the offspring of consanguineous couples, including data on the prenatal situation. METHODS: Over 20 years (1993-2012), 35,391 fetuses were examined by prenatal sonography. In 675 cases (1.9%), parents were consanguineous, with 307 couples (45.5%) related as first cousins, 368 couples (54.5%) beyond first cousins. Detailed information was retrieved on 31,710 (89.6%) fetuses, (consanguineous 568: 1.8%). RESULTS: Overall prevalence of major anomalies among fetuses with non-consanguineous parents was 2.9% (consanguineous, 10.9%; first cousins, 12.4%; beyond first cousins, 6.5%). Adjusting the overall numbers for cases having been referred because of a previous index case, the prevalences were 2.8% (non-consanguineous) and 6.1% (consanguineous) (first cousin, 8.5%; beyond first cousin, 3.9%). Further adjustment for differential rates of trisomic pregnancies indicated 2.0%/5.9% congenital anomalies (non-consanguineous/consanguineous groups), that is, a consanguinity-associated excess of 3.9%, 6.1% in first cousin progeny and 1.9% beyond first cousin. CONCLUSIONS: The prevalence of major fetal anomalies associated with consanguinity is higher than in evaluations based only on postnatal life. It is important that this information is made available in genetic counselling programmes, especially in multi-ethnic and multi-religious communities, to enable couples to make informed decisions.


Subject(s)
Consanguinity , Ethnicity/statistics & numerical data , Pregnancy Outcome/epidemiology , Adolescent , Adult , Europe/epidemiology , Female , Germany/epidemiology , Humans , Infant, Newborn , Male , Middle Aged , Pregnancy , Prevalence , Urban Population/statistics & numerical data , Young Adult
3.
Am J Hum Genet ; 88(5): 608-15, 2011 May 13.
Article in English | MEDLINE | ID: mdl-21549340

ABSTRACT

We used whole-exome sequencing to study three individuals with a distinct condition characterized by short stature, chondrodysplasia with brachydactyly, congenital joint dislocations, cleft palate, and facial dysmorphism. Affected individuals carried homozygous missense mutations in IMPAD1, the gene coding for gPAPP, a Golgi-resident nucleotide phosphatase that hydrolyzes phosphoadenosine phosphate (PAP), the byproduct of sulfotransferase reactions, to AMP. The mutations affected residues in or adjacent to the phosphatase active site and are predicted to impair enzyme activity. A fourth unrelated patient was subsequently found to be homozygous for a premature termination codon in IMPAD1. Impad1 inactivation in mice has previously been shown to produce chondrodysplasia with abnormal joint formation and impaired proteoglycan sulfation. The human chondrodysplasia associated with gPAPP deficiency joins a growing number of skeletoarticular conditions associated with defective synthesis of sulfated proteoglycans, highlighting the importance of proteoglycans in the development of skeletal elements and joints.


Subject(s)
Bone Diseases, Developmental/pathology , Joint Diseases/pathology , Mutation , Phosphoric Monoester Hydrolases/genetics , Amino Acid Sequence , Bone Diseases, Developmental/enzymology , Female , Golgi Apparatus/enzymology , Homozygote , Humans , Infant , Infant, Newborn , Joint Diseases/enzymology , Limb Deformities, Congenital/pathology , Male , Molecular Sequence Data , Nucleotides/metabolism , Phenotype , Protein Structure, Quaternary , Proteoglycans/metabolism , Sulfotransferases/metabolism , Young Adult
5.
Prenat Diagn ; 27(5): 475-8, 2007 May.
Article in English | MEDLINE | ID: mdl-17330228

ABSTRACT

OBJECTIVES: Deletions in the short arm of chromosome 12 are rare structural aberrations. Till now only ten patients with interstitial deletions are described in the literature. Here, we report on the first case detected by prenatal diagnosis. Chorionic villi sampling was performed in the 14th week of gestation, indicated by fetal abnormalities detected by ultrasound examination. Conventional cytogenetic and molecular cytogenetic techniques were applied to determine the correct karyotype of the affected fetus. RESULTS: Analysing Giemsa- and QFQ-stained chromosomes of the CVS short-term culture, a structural aberrant chromosome 12 was detected. Fluorescence in situ hybridisation with YAC-probes and CGH analysis with DNA extracted from native chorionic villi proved an interstitial deletion in the aberrant chromosome 12. The GTG-banded chromosomes of the CVS long-term culture confirmed these results. Analyses of the parental chromosomal sets yielded normal results, indicating a de novo aberration. Array CGH analysis was performed to determine accurately the deletion breakpoints. Finally, according to ISCN 2005, the karyotype could be determined as 46,XX.arr cgh 12p13.2p11.21(RP11-77I22-->RP11-144O23)x 1. CONCLUSION: The presented case shows the power of modern cytogenetic methods, allowing a more detailed diagnosis in affected individuals, and therefore, facilitating a more reliable prenatal diagnosis.


Subject(s)
Chromosome Deletion , Chromosomes, Human, Pair 12 , Prenatal Diagnosis , Abnormalities, Multiple/diagnosis , Abnormalities, Multiple/embryology , Abnormalities, Multiple/genetics , Abortion, Eugenic , Adult , Diagnosis, Differential , Female , Humans , Pregnancy , Pregnancy Trimester, First
6.
Am J Med Genet A ; 124A(1): 85-8, 2004 Jan 01.
Article in English | MEDLINE | ID: mdl-14679592

ABSTRACT

The first case of a fetal trisomy 6 mosaicism proven at 25 weeks of gestation by analysis of fetal urine cells is described. Chromosomal analysis was indicated by an ultrasonographically diagnosed heart defect at 21 weeks of gestation. The chromosomal aberration was detected in amniotic fluid cells while fetal blood cells showed a normal chromosome set. At term a boy with normal growth parameter was born. In addition to the expected heart defect, malformations of hands and feet were present.


Subject(s)
Chromosomes, Human, Pair 6/genetics , Foot Deformities, Congenital/genetics , Hand Deformities, Congenital/genetics , Mosaicism , Prenatal Diagnosis , Trisomy/diagnosis , Adult , Female , Foot Deformities, Congenital/pathology , Hand Deformities, Congenital/pathology , Heart Defects, Congenital/genetics , Humans , Infant, Newborn , Male , Phenotype , Pregnancy , Pregnancy Trimester, Second
SELECTION OF CITATIONS
SEARCH DETAIL
...