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.

[1] Manifestations include enlarged viscera, hepatomegaly, diabetes, short stature and cranial hyperostosis.

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