Congenital idiopathic hypothyroidism (Q95625): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Changed label, description and/or aliases in pt-br, en
‎Changed an Item
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/720883616 / rank
 
Normal rank

Revision as of 11:26, 16 August 2026

Idiopathic congenital hypothyroidism is a type of primary congenital hypothyroidism whose cause is unknown. Clinical manifestations are those of other forms of congenital hypothyroidism. Goitre is always absent. Ultrasound examination and thyroid scintigraphy show a thyroid gland of normal shape and size in the normal, eutopic location. Idiopathic congenital hypothyroidism can be diagnosed after exclusion of the known causes of congenital hypothyroidism.
Language Label Description Also known as
default for all languages
ID_720883616
    English
    Congenital idiopathic hypothyroidism
    Idiopathic congenital hypothyroidism is a type of primary congenital hypothyroidism whose cause is unknown. Clinical manifestations are those of other forms of congenital hypothyroidism. Goitre is always absent. Ultrasound examination and thyroid scintigraphy show a thyroid gland of normal shape and size in the normal, eutopic location. Idiopathic congenital hypothyroidism can be diagnosed after exclusion of the known causes of congenital hypothyroidism.

      Statements