Rare Diseases Symptoms Automatic Extraction

Dermatologic, periodontal, and skeletal manifestations of Haim-Munk syndrome in two siblings.

[papillon-lefèvre syndrome]

Haim-Munk syndrome is an extremely rare autosomal recessive disorder of keratinization characterized clinically by palmoplantar hyperkeratosis, severe early onset periodontitis, onychogryphosis, pes planus, arachnodactyly, and acro-osteolysis. Recently, germline mutations in the lysosomal protease cathepsin C gene have been identified as the underlying genetic defect in Haim-Munk syndrome and in the clinically related disorders, Papillon-Lefèvre syndrome and prepubertal periodontitis.

Diseases presenting "extremely rare autosomal" symptom

  • dentin dysplasia
  • papillon-lefèvre syndrome

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