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Combined pituitary hormone deficiencies, genetic form

MONDO:0013099

Congenital hypopituitarism is characterized by multiple pituitary hormone deficiency, including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies, due to mutations of pituitary transcription factors involved in pituitary ontogenesis. Congenital hypopituitarism is rare compared with the high incidence of hypopituitarism induced by pituitary adenomas, transsphenoidal surgery or radiotherapy.

Also known as: familial congenital hypopituitarism, genetic hypopituitarism, multiple pituitary hormone deficiencies, genetic forms, pituitary hormone deficiency, combined, combined pituitary hormone deficiencies, genetic forms, familial hypopituitarism

43 clinical trials for this condition and its sub-types, 1 tagged with Combined pituitary hormone deficiencies, genetic form itself.

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