Pseudoadrenoleukodystrophy: A rare disorder where an enzyme deficiency (Acyl-CoA Oxidase) results in symptoms such as seizures, apnea, delayed psychomotor retardation and neurological deterioration.
More detailed information about the symptoms,
causes, and treatments of Pseudoadrenoleukodystrophy is available below.
Symptoms of Pseudoadrenoleukodystrophy
See full list of 26
symptoms of Pseudoadrenoleukodystrophy
Home Diagnostic Testing
Home medical testing related to Pseudoadrenoleukodystrophy:
- Sleep Disorders: Home Testing
- Nerve Neuropathy: Related Home Testing:
Wrongly Diagnosed with Pseudoadrenoleukodystrophy?
Pseudoadrenoleukodystrophy: Related Patient Stories
Review possible medical complications related to Pseudoadrenoleukodystrophy:
Causes of Pseudoadrenoleukodystrophy
Read more about causes of Pseudoadrenoleukodystrophy.
Less Common Symptoms of Pseudoadrenoleukodystrophy
See full list of 7
occasional symptoms of Pseudoadrenoleukodystrophy
Pseudoadrenoleukodystrophy: Undiagnosed Conditions
Commonly undiagnosed diseases in related medical categories:
Misdiagnosis and Pseudoadrenoleukodystrophy
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Read more about Misdiagnosis and Pseudoadrenoleukodystrophy
Pseudoadrenoleukodystrophy: Research Doctors & Specialists
Research related physicians and medical specialists:
Other doctor, physician and specialist research services:
More Pseudoadrenoleukodystrophy animations & videos
Statistics for Pseudoadrenoleukodystrophy
Pseudoadrenoleukodystrophy: Broader Related Topics
Types of Pseudoadrenoleukodystrophy
User Interactive Forums
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Definitions of Pseudoadrenoleukodystrophy:
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Pseudoadrenoleukodystrophy as a "rare disease".
Source - Orphanet
Contents for Pseudoadrenoleukodystrophy: