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PMD
Introduction: PMD
Description of PMD
PMD (medical condition):
Rare brain myelin disorder.
See also Pelizaeus-Merzbacher Disease:
»Introduction: Pelizaeus-Merzbacher Disease
»Symptoms of Pelizaeus-Merzbacher Disease
PMD: Rare Disease
Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)
PMD is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that PMD, or a subtype of PMD,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list PMD as a "rare disease".
Source - Orphanet
PMD as a Disease
PMD: Another name for Pelizaeus-Merzbacher Disease (or close medical condition association).
»Introduction: Pelizaeus-Merzbacher Disease
»Symptoms of Pelizaeus-Merzbacher Disease
PMD: PMD is listed as a type of (or associated with) the following medical conditions in our database: leukodystrophies, Brain conditions
Symptoms of PMD (Pelizaeus-Merzbacher Disease)
Some of the symptoms of PMD incude:
- Symptoms in infants include:
- Symptoms in adults include:
See full list of 16 symptoms of PMD (Pelizaeus-Merzbacher Disease)
PMD: Article Excerpts about Pelizaeus-Merzbacher Disease
Pelizaeus-Merzbacher disease is a rare, progressive, degenerative central nervous system disorder in which coordination, motor abilities, and intellectual function deteriorate. The disease is one of a group of genetic disorders called the leukodystrophies that affect growth of the myelin sheath, the fatty covering--which acts as an insulator--on nerve fibers in the brain. (Source: excerpt from NINDS Pelizaeus-Merzbacher Disease Information Page: NINDS)
Terms associated with PMD:
Terms Similar to PMD:
Source - NIH
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