XY PURE GONADAL (TESTICULAR) DYSGENESIS - BRIEF REPORT OF A FAMILIAL CASE

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3046778 32 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
XY PURE GONADAL (TESTICULAR) DYSGENESIS - BRIEF REPORT OF A FAMILIAL
CASE
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Three sisters were found to have pure gonadal dysgenesis. The diagnosis
was confirmed by the finding of streak gonads and biopsy during
laparotomy. Cytogenetic studies in a number of different tissues showed
a normal male (46,XY) karyotype, none of which revealed signs of Turner
syndrome. Histologically, no evidence of testicular differentiation was
seen in any of the streak gonads examined. Hormonal studies, carried out
in all three sisters, indicated elevated serum gonadotropin levels with
normal female testosterone levels. Transmission of this disorder of
testicular development by genes on the X chromosome or an autosome, as
described in other genetic disorders of male development, is the most
likely mode of inheritance.
Έτος δημοσίευσης:
1994
Συγγραφείς:
CARDAMAKIS, E
CREATSAS, G
DELIGEOROGLOU, E
ARAVANTINOS, D
Περιοδικό:
ADOLESCENT AND PEDIATRIC GYNECOLOGY
Εκδότης:
Springer-Verlag
Τόμος:
7
Αριθμός / τεύχος:
1
Σελίδες:
34-37
Λέξεις-κλειδιά:
GONADAL DYSGENESIS; SWYER SYNDROME; STREAK GONADS; AMENORRHEA
Επίσημο URL (Εκδότης):
DOI:
10.1016/S0932-8610(12)80176-9
Το ψηφιακό υλικό του τεκμηρίου δεν είναι διαθέσιμο.