Nivelon-Nivelon-Mabille syndrome: A very rare syndrome characterized mainly by severe dwarfism, abnormal bone development and central nervous system and eye problems. More detailed information about the symptoms, causes, and treatments of Nivelon-Nivelon-Mabille syndrome is available below.
See full list of 23 symptoms of Nivelon-Nivelon-Mabille syndrome
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Types of Nivelon-Nivelon-Mabille syndrome
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Nivelon-Nivelon-Mabille syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Nivelon-Nivelon-Mabille syndrome, or a subtype of Nivelon-Nivelon-Mabille syndrome,
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 Nivelon-Nivelon-Mabille syndrome as a "rare disease".
Source - Orphanet
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