Combined pituitary hormone deficiencies, genetic forms

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Combined pituitary hormone deficiencies, genetic forms

Synonyms: Familial congenital hypopituitarism | Multiple pituitary hormone deficiencies, genetic forms

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.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024

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Combined pituitary hormone deficiencies, genetic forms?

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