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VLCAD deficiency

VLCAD deficiency: Introduction

VLCAD deficiency: A rare condition that is characterised by cardiomyopathy, fatty liver, skeletal myopathy, pericardial effusions, ventricular arrhythmias, and sudden death. More detailed information about the symptoms, causes, and treatments of VLCAD deficiency is available below.

Symptoms of VLCAD deficiency

Wrongly Diagnosed with VLCAD deficiency?

VLCAD deficiency: Related Patient Stories

VLCAD deficiency: Deaths

Read more about Deaths and VLCAD deficiency.

Causes of VLCAD deficiency

Read more about causes of VLCAD deficiency.

Disease Topics Related To VLCAD deficiency

Research the causes of these diseases that are similar to, or related to, VLCAD deficiency:

Misdiagnosis and VLCAD deficiency

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as more »

Evidence Based Medicine Research for VLCAD deficiency

Medical research articles related to VLCAD deficiency include:

Click here to find more evidence-based articles on the TRIP Database

Research about VLCAD deficiency

Visit our research pages for current research about VLCAD deficiency treatments.

Statistics for VLCAD deficiency

VLCAD deficiency: Broader Related Topics

User Interactive Forums

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

Definitions of VLCAD deficiency:

VLCAD deficiency is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that VLCAD deficiency, or a subtype of VLCAD deficiency, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list VLCAD deficiency as a "rare disease".
Source - Orphanet


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