Katz syndrome
| Hyperostosis frontalis interna | |
|---|---|
 | |
| Hyperostosis frontalis interna in a 74-year-old woman | |
| Classification and external resources |
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]
Symptoms
Manifestations include enlarged viscera, hepatomegaly, diabetes, short stature and cranial hyperostosis.
References
- ↑ 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
This article is issued from Wikipedia - version of the 4/16/2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.