| 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
Manifestations include enlarged viscera, hepatomegaly, diabetes, short stature and cranial hyperostosis.[ citation needed]
Diagnosis
![[icon]](/info/en/?search=File:Wiki_letter_w_cropped.svg){kind=small} | This section is empty. You can help by
adding to it. (September 2017) |
Treatment
|
| This section is empty. You can help by
adding to it. (September 2017) |
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 genetic disorder article is a stub. You can help Wikipedia by expanding it. |
| 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
Manifestations include enlarged viscera, hepatomegaly, diabetes, short stature and cranial hyperostosis.[ citation needed]
Diagnosis
|
| This section is empty. You can help by
adding to it. (September 2017) |
Treatment
|
| This section is empty. You can help by
adding to it. (September 2017) |
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 genetic disorder article is a stub. You can help Wikipedia by expanding it. |