Congenital Hypothyroidism (CH)

Gene
TSHB
Location
1p13
Disease
Congenital Hypothyroidism (CH)
Description
Congenital hypothyroidism is a condition that affects infants from birth (congenital) and results from a partial or complete loss of thyroid function (hypothyroidism).
Signs and Symptoms
If untreated, congenital hypothyroidism can lead to intellectual disability and abnormal growth. Other genes that may cause congenital hypothyroidism include the DUOX2, PAX8, SLC5A5, TG, TPO, and TSHR genes.
Type
Endocrine Disorders
Category
Core

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