Adrenomyodystrophy

MONDO:0010288

Adrenomyodystrophy 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.

Also known as: adrenomyodystrophy

2 clinical trials for this condition and its sub-types, 0 tagged with Adrenomyodystrophy itself.

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Where it sits in the disease tree

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Part of

↑ Adrenal gland disorder (352)

Including sub-types (2) Tagged with Adrenomyodystrophy (0)

Trials to join now! 1 Not yet recruiting 1

Tiny trial to see if a dye helps adrenal surgery

Knowledge-focused Not yet recruiting

This study will look at 12 people having surgery to remove an adrenal gland (adrenalectomy) using robotic or laparoscopic methods. Some surgeries will use a green dye called Indocyanine Green (ICG) to help the surgeon see better, while others will not. The main goal is to track c…

Sponsor: University of Roma La Sapienza • Aim: Knowledge-focused

Last updated Jun 27, 2026 12:32 UTC

Adrenomyodystrophy

Where it sits in the disease tree

Tiny trial to see if a dye helps adrenal surgery