Lutz-Richner-Landolt syndrome: A rare disorder involving kidney and biliary abnormalities. More detailed information about the symptoms, causes, and treatments of Lutz-Richner-Landolt syndrome is available below.
See full list of 15 symptoms of Lutz-Richner-Landolt syndrome
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Prognosis for Lutz-Richner-Landolt syndrome: death within months
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Types of Lutz-Richner-Landolt syndrome
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Lutz-Richner-Landolt syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Lutz-Richner-Landolt syndrome, or a subtype of Lutz-Richner-Landolt 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 Lutz-Richner-Landolt syndrome as a "rare disease".
Source - Orphanet
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