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Up to: Hereditary neurological disease · Congenital nervous system disorder · Congenital hypogonadotropic hypogonadism · Hypopituitarism

Combined pituitary hormone deficiencies, genetic form

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.

1 trial tagged with this condition →

Isolated congenital growth hormone deficiency 38 trials Sub-types →
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Congenital isolated adrenocorticotropic hormone deficiency 1 trial
Pituitary hormone deficiency, combined, 1 1 trial
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Non-acquired combined pituitary hormone deficiency with spine abnormalities 0 trials
Pituitary hormone deficiency, combined or isolated, 8 0 trials
Pituitary hormone deficiency, combined, 6 0 trials
Short stature-pituitary and cerebellar defects-small sella turcica syndrome 0 trials