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NADH cytochrome B5 reductase deficiency

NADH cytochrome B5 reductase deficiency: Introduction

NADH cytochrome B5 reductase deficiency: A very rare syndrome caused by a genetic anomaly resulting in an enzyme deficiency (NADH cytochrome B5 reductase). More detailed information about the symptoms, causes, and treatments of NADH cytochrome B5 reductase deficiency is available below.

Symptoms of NADH cytochrome B5 reductase deficiency

Wrongly Diagnosed with NADH cytochrome B5 reductase deficiency?

NADH cytochrome B5 reductase deficiency: Complications

Read more about complications of NADH cytochrome B5 reductase deficiency.

Causes of NADH cytochrome B5 reductase deficiency

Read more about causes of NADH cytochrome B5 reductase deficiency.

Misdiagnosis and NADH cytochrome B5 reductase deficiency

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NADH cytochrome B5 reductase deficiency: Broader Related Topics

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Definitions of NADH cytochrome B5 reductase deficiency:

NADH cytochrome B5 reductase deficiency is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that NADH cytochrome B5 reductase deficiency, or a subtype of NADH cytochrome B5 reductase 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 NADH cytochrome B5 reductase deficiency as a "rare disease".
Source - Orphanet

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More information about NADH cytochrome B5 reductase deficiency

  1. NADH cytochrome B5 reductase deficiency: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Complications
 

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