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Non-acquired combined pituitary hormone deficiency

MedGen UID:
1842250
Concept ID:
C5680091
Disease or Syndrome
Synonyms: Congenital combined pituitary hormone deficiency; congenital combined pituitary hormone deficiency; Congenital hypopituitarism; congenital hypopituitarism; non-acquired combined pituitary hormone deficiency
 
Monarch Initiative: MONDO:0018762
Orphanet: ORPHA467

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. [from ORDO]

Recent clinical studies

Etiology

Khadilkar VV, Prasad HK, Ekbote VH, Rustagi VT, Singh J, Chiplonkar SA, Khadilkar AV
Indian J Pediatr 2015 May;82(5):404-9. Epub 2014 Apr 29 doi: 10.1007/s12098-014-1412-9. PMID: 24777622

Therapy

Khadilkar VV, Prasad HK, Ekbote VH, Rustagi VT, Singh J, Chiplonkar SA, Khadilkar AV
Indian J Pediatr 2015 May;82(5):404-9. Epub 2014 Apr 29 doi: 10.1007/s12098-014-1412-9. PMID: 24777622

Prognosis

Khadilkar VV, Prasad HK, Ekbote VH, Rustagi VT, Singh J, Chiplonkar SA, Khadilkar AV
Indian J Pediatr 2015 May;82(5):404-9. Epub 2014 Apr 29 doi: 10.1007/s12098-014-1412-9. PMID: 24777622

Clinical prediction guides

Khadilkar VV, Prasad HK, Ekbote VH, Rustagi VT, Singh J, Chiplonkar SA, Khadilkar AV
Indian J Pediatr 2015 May;82(5):404-9. Epub 2014 Apr 29 doi: 10.1007/s12098-014-1412-9. PMID: 24777622

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