Combined pituitary hormone deficiencies, genetic forms

Orpha code: 95494OMIM code: 613986

Definition

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.

Disease data
Classification

Disease

Synonyms
Familial congenital hypopituitarism
Rodzinna wrodzona niedoczynność przysadki
Złożone niedobory hormonów przysadki, formy genetyczne
Multiple pituitary hormone deficiencies, genetic forms
ORPHA code
95494
OMIM code
613986
ICD10 code
E23.0
ICD11 code
-

No additional description.

Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl