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. | |||
| description / en | description / en | ||
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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_866175475 |
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| English | 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. |
