Pregled bibliografske jedinice broj: 403501
Report of fertility in woman with predominantly 46, XY karyotype in family with multiple disorders of sexual development : Review of Prismatic Case
Report of fertility in woman with predominantly 46, XY karyotype in family with multiple disorders of sexual development : Review of Prismatic Case // Mount Sinai Journal of Medicine, 75 (2008), 2; 168-169 doi:10.1002/msj.20046 (podatak o recenziji nije dostupan, pismo uredniku, znanstveni)
CROSBI ID: 403501 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Report of fertility in woman with predominantly 46, XY karyotype in family with multiple disorders of sexual development : Review of Prismatic Case
Autori
Dumić, Miroslav ; Lin-Su, Karen ; Leibel, Natasha I. ; Ciglar, Srećko ; Vinci, Giovanna ; Lasan, Ružica ; Nimkarn, Saroj ; Wilson, Jean D. ; McElreavey, Ken ; New, Maria I.
Izvornik
Mount Sinai Journal of Medicine (0027-2507) 75
(2008), 2;
168-169
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, pismo uredniku, znanstveni
Ključne riječi
fertile 46; XY female; sexual differentiation; intersex; complete gonadal dysgenesis; genetics
Sažetak
We report herein a remarkable family in which the mother of a woman with 46, XY complete gonadal dysgenesis was found to have a 46, XY karyotype in peripheral lymphocytes, mosaicism in cultured skin fibroblasts (80% 46, XY and 20% 45, X) and a predominantly 46, XY karyotype in the ovary (93% 46, XY and 6% 45, X). Patients: A 46, XY mother who developed as a normal woman, underwent spontaneous puberty, reached menarche, menstruated regularly, experienced two unassisted pregnancies, and gave birth to a 46, XY daughter with complete gonadal dysgenesis. Results: Evaluation of the Y chromosome in the daughter and both parents revealed that the daughter inherited her Y chromosome from her father. Molecular analysis of the genes SOX9, SF1, DMRT1, DMRT3, TSPYL, BPESC1, DHH, WNT4, SRY and DAX1 revealed normal coding sequences in both the mother and daughter. An extensive family pedigree across four generations revealed multiple other family members with ambiguous genitalia and infertility in both phenotypic males and females and the mode of inheritance of the phenotype was strongly suggestive of X-linkage. Conclusions: The range of phenotypes observed in this unique family suggests that there may be transmission of a mutation in a novel sex determining gene or in a gene that predisposes to chromosomal mosaicism
Izvorni jezik
Engleski
Znanstvena područja
Biologija, Temeljne medicinske znanosti, Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
108-0000000-0359 - Nasljedne endokrine bolesti u djece (Dumić, Miroslav, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb,
Klinički bolnički centar Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE