Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Isabel Inácio"'
Publikováno v:
JCRPE, Vol 15, Iss 1, Pp 86-89 (2023)
The coexistence of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency and Turner syndrome (TS) is rare. We report on a 6-year-old Portuguese girl with mosaic TS [45,XO(39)/47,XXX(21)] presenting with premature pubarche at the age o
Externí odkaz:
https://doaj.org/article/5da0d6f8c59f46a38390e32bc8cbc531
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. 15:86-89
Coexistence of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency and Turner Syndrome (TS) is rare. We report a 6-year-old Portuguese girl with mosaic TS [45,XO(39)/47,XXX(21)] presented with premature pubarche at the age of 5 year