Katz syndrome
| Katz syndrome | |
|---|---|
| Other names | Hyperostosis frontalis interna |
 | |
| Hyperostosis frontalis interna in a 74-year-old woman | |
| Specialty | Medical genetics |
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 and signs
[edit]Manifestations include enlarged viscera, hepatomegaly, diabetes, short stature and cranial hyperostosis.[citation needed]
Diagnosis
[edit]![[icon]](/wiki/File:Wiki_letter_w_cropped.svg){kind=small} | This section is empty. You can help by adding to it. (September 2017) |
Treatment
[edit] | This section is empty. You can help by adding to it. (September 2017) |
References
[edit]- ^ 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 genetic disorder article is a stub. You can help Wikipedia by expanding it. |