Category
page 1Palmoplantar keratodermas
Mal de Meleda
human disease
palmoplantar keratosis
keratosis characterized by abnormal thickening of the palms and the soles
Papillon-Lefevre disease
Human disease
Haim–Munk syndrome
Haim-Munk syndrome (HMS) is characterized by palmoplantar hyperkeratosis, severe early-onset periodontitis, onychogryposis, pes planus, arachnodactyly and acroosteolysis
Clouston syndrome
Human disease
Naxos disease
Naxos disease is a recessively inherited condition with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) and a cutaneous phenotype, characterised by peculiar woolly hair and palmoplantar keratoderma
keratitis–ichthyosis–deafness syndrome
human disease
tyrosinemia type II
tyrosinemia that has material basis in deficiency of hepatic tyrosine aminotransferase located in the liver and is characterized by keratitis, painful palmoplantar hyperkeratosis, mental retardation, and elevated serum tyrosine levels