Haim–Munk syndrome
Haim–Munk syndrome | |
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Classification and external resources | |
ICD-10 | Q82.8 |
OMIM | 245010 |
Haim–Munk syndrome (also known as "Palmoplantar keratoderma with periodontitis and arachnodactyly and acro-osteolysis"[1]) is a cutaneous condition caused by a mutation in the Cathepsin C gene.[1] It was named after Dr. Salim Haim and Dr. Munk.[2] l
See also
- Ichthyosis–sclerosing cholangitis syndrome
- List of cutaneous conditions
- List of dental abnormalities associated with cutaneous conditions