Molecular analysis of SRY gene in patients with mixed gonadal dysgenesis

Citation
F. Alvarez-nava et al., Molecular analysis of SRY gene in patients with mixed gonadal dysgenesis, ANN GENET, 44(3), 2001, pp. 155-159
Citations number
37
Categorie Soggetti
Molecular Biology & Genetics
Journal title
ANNALES DE GENETIQUE
ISSN journal
00033995 → ACNP
Volume
44
Issue
3
Year of publication
2001
Pages
155 - 159
Database
ISI
SICI code
0003-3995(200107/09)44:3<155:MAOSGI>2.0.ZU;2-X
Abstract
Mixed gonadal dysgenesis (MGD) includes a group of heterogeneous conditions consisting of a dysgenetic testis with a streak gonad. MGD is probably due to a disturbance in testicular determination/differentiation. The objectiv e. of this study is to analyze the SRY ne in MGD patients. A molecular inve stigation was undertaken in sixteen patients with this disorder in an attem pt to determine mutations in SRY through polymerase chain reaction, single strand conformational polymorphism and direct sequencing. Eleven patients s howed 45,X/46,XY and five 46,XY karyotype. Mutations in SRY gene were shown to be absent in these patients. This study confirms the findings of other studies. The etiology of MGD is heterogeneous, and cytogenetics mosaicism t ypically seen in these patients may be a cause of this condition, although, the presence of mutations in testicular organizing genes downstream of SRY is still to rule out. (C) 2001 Editions scientifiques et medicales Elsevie r SAS.