Rambaud-Galian syndrome: A very rare syndrome characterized by the progressive deposition of a substance called hyaline in blood vessels of the digestive tract and kidneys. Calcification of the brain is also present. More detailed information about the symptoms, causes, and treatments of Rambaud-Galian syndrome is available below.
See full list of 16 symptoms of Rambaud-Galian syndrome
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Read more about Misdiagnosis and Rambaud-Galian syndrome
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Types of Rambaud-Galian syndrome
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Rambaud-Galian syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Rambaud-Galian syndrome, or a subtype of Rambaud-Galian 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 Rambaud-Galian syndrome as a "rare disease".
Source - Orphanet
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