Genetic transient congenital hypothyroidism
ORPHA:226316· ICD-10 P72.2
Definition
Genetic transient congenital hypothyroidism is a rare, thyroid disease characterized by a gene mutation induced, temporary deficiency of thyroid hormones at birth, which later reverts to normal with or without replacement therapy in the first few months or years of life.
- Inheritance
- Autosomal recessive
- Age of onset
- Infancy, Neonatal