Congenital hypothyroidism due to developmental anomaly
ORPHA:95711· ICD-10 E03.1
Definition
Thyroid dysgenesis is a type of primary congenital hypothyroidism, a permanent thyroid hormone deficiency that is present from birth.
- Prevalence
- 1-5 / 10 000
ORPHA:95711· ICD-10 E03.1
Thyroid dysgenesis is a type of primary congenital hypothyroidism, a permanent thyroid hormone deficiency that is present from birth.