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Peroxisome biogenesis disorders

Peroxisome biogenesis disorders: Introduction

Peroxisome biogenesis disorders: A group of inherited disorders involving the absence or dysfunction of one or more peroxisomal enzymes. Peroxisomes are numerous tiny organs within the cell which are involved in a large number of the body's biochemical reactions. More detailed information about the symptoms, causes, and treatments of Peroxisome biogenesis disorders is available below.

Symptoms of Peroxisome biogenesis disorders

  • Dysmorphic craniofacial features
  • Neurological dysfunction
  • Severe lack of muscle tone
  • Excessive muscle tone in extremities
  • Seizures
  • more symptoms...»

See full list of 12 symptoms of Peroxisome biogenesis disorders

Disease Topics Related To Peroxisome biogenesis disorders

Research the causes of these diseases that are similar to, or related to, Peroxisome biogenesis disorders:

Evidence Based Medicine Research for Peroxisome biogenesis disorders

Medical research articles related to Peroxisome biogenesis disorders include:

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Reseach about Peroxisome biogenesis disorders

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Definitions of Peroxisome biogenesis disorders:

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


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