Nonacquired combined hypopituitarism (Q97189): Difference between revisions

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Hipopituitarismo congênito é caracterizado por deficiência múltipla dos hormônios hipofisários, incluindo deficiência somatotrófica, tireotrófica, lactotrófica, corticotrófica ou gonadotrófica, devido a mutações em fatores de transcrição hipofisários envolvidos na ontogênese hipofisária.
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Congenital hypopituitarism is characterised by multiple pituitary hormone deficiency, including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies, due to mutations of pituitary transcription factors involved in pituitary ontogenesis.

Revision as of 13:13, 16 August 2026

Congenital hypopituitarism is characterised by multiple pituitary hormone deficiency, including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies, due to mutations of pituitary transcription factors involved in pituitary ontogenesis.
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    Nonacquired combined hypopituitarism
    Congenital hypopituitarism is characterised by multiple pituitary hormone deficiency, including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies, due to mutations of pituitary transcription factors involved in pituitary ontogenesis.

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