Haim-Munk syndrome
What is Haim-Munk syndrome?
Haim-Munk syndrome (HMS) is characterized by palmoplantar hyperkeratosis, severe early-onset periodontitis, onychogryposis, pes planus, arachnodactyly and acroosteolysis.
Other condition names
- Keratosis palmoplantaris-periodontopathia-onychogryposis syndrome
- Palmoplantar hyperkeratosis-periodontopathia-onychogryposis syndrome
- Palmoplantar keratoderma-periodontopathia-onychogryposis syndrome
Inheritance type
Autosomal recessive
Prevalence
- Worldwide: <1 in 1,000 000
Age of Onset
- Childhood
- Infancy
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on "https://www.orphadata.com". Data version 1.3.16 / 4.1.7.