Saito-Kuba-Tsuruta syndrome: A very rare syndrome characterized by kidney abnormalities and an abnormal calf bone or forearm bone (ulna). Only a few cases of the syndrome have been reported. More detailed information about the symptoms, causes, and treatments of Saito-Kuba-Tsuruta syndrome is available below.
See full list of 20 symptoms of Saito-Kuba-Tsuruta syndrome
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Saito-Kuba-Tsuruta syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Saito-Kuba-Tsuruta syndrome, or a subtype of Saito-Kuba-Tsuruta 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 Saito-Kuba-Tsuruta syndrome as a "rare disease".
Source - Orphanet
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