Combined pituitary hormone deficiencies, genetic form
MONDO:0013099Congenital 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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Sub-types of Combined pituitary hormone deficiencies, genetic form
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7 sub-types
- Isolated growth hormone deficiency type IA 0 trials
- Isolated growth hormone deficiency type IB 0 trials
- Isolated growth hormone deficiency type II 0 trials
- Isolated growth hormone deficiency type III 0 trials Sub-types →
- Isolated growth hormone deficiency, type 4 0 trials
- Isolated growth hormone deficiency, type 5 0 trials
- Short stature due to growth hormone qualitative anomaly 0 trials
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Panhypopituitarism 2 trials
2 sub-types
- Panhypopituitarism, X-linked 0 trials
- Pituitary hormone deficiency, combined, 2 0 trials
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Septooptic dysplasia 1 trial
2 sub-types
- Congenital absence of septum pellucidum 0 trials
- Pagon stephan syndrome 0 trials