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Neonatal adrenoleukodystrophy (medical condition): A rare inherited disorder involving the adrenal glands, testes and certain parts of the brain (white matter). It is a less severe form of leukodystrophy where an abnormality within the body cells prevents the metabolism of certain fats (long chain fatty acids).
See also:
Adrenoleukodystrophy, autosomal, neonatal form:
»Introduction: Adrenoleukodystrophy, autosomal, neonatal form
»Symptoms of Adrenoleukodystrophy, autosomal, neonatal form
These medical condition or symptom topics may be relevant to medical information for Neonatal adrenoleukodystrophy:
Neonatal adrenoleukodystrophy is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Neonatal adrenoleukodystrophy, or a subtype of Neonatal adrenoleukodystrophy,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Neonatal adrenoleukodystrophy: Another name for Adrenoleukodystrophy, autosomal, neonatal form (or close medical condition association).
»Introduction: Adrenoleukodystrophy, autosomal, neonatal form
»Symptoms of Adrenoleukodystrophy, autosomal, neonatal form
Some of the symptoms of Neonatal adrenoleukodystrophy incude:
These medical disease topics may be related to Neonatal adrenoleukodystrophy:
Source - NIH
Search to find out more about Neonatal adrenoleukodystrophy:
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