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Adrenomyodystrophy

MedGen UID:
337494
Concept ID:
C1846044
Disease or Syndrome
Synonym: ADRENOMYODYSTROPHY
SNOMED CT: Adrenomyodystrophy (763311001)
Modes of inheritance:
Unknown inheritance
MedGen UID:
989040
Concept ID:
CN307042
Finding
Source: Orphanet
Hereditary clinical entity whose mode of inheritance is unknown.
 
Monarch Initiative: MONDO:0010288
OMIM®: 300270
Orphanet: ORPHA977

Definition

An extremely rare genetic endocrine disease with characteristics of primary adrenal insufficiency, dystrophic myopathy, hepatic steatosis, severe psychomotor delay, megalocornea, failure to thrive, chronic constipation, and terminal bladder ectasia which can lead to death. There have been no further descriptions in the literature since 1982. [from SNOMEDCT_US]

Recent clinical studies

Diagnosis

von Petrykowski W, Beckmann R, Böhm N, Ketelsen UP, Ropers HH, Sauer M
Helv Paediatr Acta 1982 Sep;37(4):387-400. PMID: 7153060

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