Hypotonia-cystinuria syndrome: A genetic disorder characterized by reduced muscle tone, growth hormone deficiency and unusual facial appearance. Failure to thrive occurs during the first years of life but is replaced by rapid weight gain in later childhood. This syndrome is a milder form of the 2p21 deletion syndrome. More detailed information about the symptoms, causes, and treatments of Hypotonia-cystinuria syndrome is available below.
See full list of 19 symptoms of Hypotonia-cystinuria syndrome
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