A condition that affects infants from birth (congenital) and results from a partial or complete loss of thyroid function (hypothyroidism). Congenital …
Thyroid/Adrenal/Other Gland Disorders
CAH
An inherited disorder caused by mutations in the CYP21A2 gene. All types of 21-hydroxylase deficiency interfere with the production of cortisol and …
Congenital Adrenal Hyperplasia
An inherited disorder caused by mutations in the CYP21A2 gene. All types of 21-hydroxylase deficiency interfere with the production of cortisol and …