An inherited disorder caused by mutations in the CYP21A2 gene. All types of 21-hydroxylase deficiency interfere with the production of cortisol and aldosterone.
Congenital Hypothyroidism (CH)
A condition that affects infants from birth (congenital) and results from a partial or complete loss of thyroid function (hypothyroidism). Congenital hypothyroidism occurs when the thyroid gland fails to develop or function properly.
Cystic Fibrosis (CF)
An inherited disease of the way our body uses chloride a chemical found in salt which affects body systems that make or use mucus such as our lungs and GI tract.
