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Katz syndrome : ウィキペディア英語版 | Katz syndrome
Katz Syndrome is a rare congenital disorder, presenting as a polymalformative syndrome characterized by enlarged viscera, hepatomegaly, diabetes, and skeletal anomalies that result in a short stature, cranial hyperostosis, and typical facial features. It is probably a variant of the autosomal recessive type of Craniometaphyseal Dysplasia.〔Bruno Bissonnette, Igor Luginbuehl, Bruno Marciniak, Bernard J. Dalens (eds.): ''Syndromes: Rapid Recognition and Perioperative Implications'' (McGraw-Hill Companies, 2006) ISBN 0-07-135455-7〕 ==Symptoms== Manifestations include enlarged viscera, hepatomegaly, diabetes, short stature and cranial hyperostosis.
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