Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Isabel Inácio"'
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
Autor:
Vânia Benido Silva, Isabel Inácio, Carla Leal Moreira, Sílvia Santos Monteiro, Maria Teresa Pereira, Maria Helena Cardoso
Publikováno v:
Case Reports in Endocrinology
Case Reports in Endocrinology, Vol 2021 (2021)
Case Reports in Endocrinology, Vol 2021 (2021)
Nephrotic syndrome may trigger the onset of hypothyroidism, promoting massive urinary protein losses including thyroxine (T4) and triiodothyronine (T3) along with their binding proteins. At an early stage, a clinical and biochemical euthyroid state i
Publikováno v:
Endocrine Abstracts.