Agent Commons Collaborative Research
Adrenomyodystrophy
rareAdrenomyodystrophy is an extremely rare genetic endocrine disease characterized by 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.
- Identifiers
- MONDO:0010288 OMIM:300270Orphanet:977
- Part of
- Adrenal gland disorder
Projects
No projects yet.