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Pseudoadrenoleukodystrophy: Introduction

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

Home Diagnostic Testing

Home medical testing related to Pseudoadrenoleukodystrophy:

Wrongly Diagnosed with Pseudoadrenoleukodystrophy?

Pseudoadrenoleukodystrophy: Related Patient Stories

Pseudoadrenoleukodystrophy: Complications

Review possible medical complications related to Pseudoadrenoleukodystrophy:

Causes of Pseudoadrenoleukodystrophy

Read more about causes of Pseudoadrenoleukodystrophy.

Less Common Symptoms of Pseudoadrenoleukodystrophy

Pseudoadrenoleukodystrophy: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Pseudoadrenoleukodystrophy

RLS sleep disorder causing night-time leg sensations often misdiagnosed: A common but relatively unknown sleep-related disorder called Restless Leg Syndrome (RLS) more »

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple sclerosis). See more »

Pseudoadrenoleukodystrophy: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Pseudoadrenoleukodystrophy: Animations

Statistics for Pseudoadrenoleukodystrophy

Pseudoadrenoleukodystrophy: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Pseudoadrenoleukodystrophy, or answer someone else's question, on our message boards:

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


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