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Keratosis palmoplantaris with periodontopathia and onychogryposis

Rare autosomal recessive disorder characterized by congenital PALMOPLANTAR KERATOSIS, flatfoot, onychogryphosis, PERIODONTITIS, ARACHNODACTYLY, and ACROOSTEOLYSIS.
Also Known As:
Cochin Jewish disorder; Haim-Munk syndrome
Networked: 9 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Erciyas, A Fuat: 1 article (07/2010)
2. Inaloz, Serhat: 1 article (07/2010)
3. Faraz, Farrukh: 1 article (07/2010)
4. Lamba, Arundeep K: 1 article (07/2010)
5. Pahwa, Priyanka: 1 article (07/2010)
6. Tandon, Shruti: 1 article (07/2010)
7. Erciyas, Kamile: 1 article (07/2010)
8. Natarajan, Karthika: 1 article (05/2010)
9. Thiagarajan, S: 1 article (05/2010)
10. Rai, Reena: 1 article (05/2010)

Related Diseases

1. Arachnodactyly
2. Acro-Osteolysis (Acroosteolysis)
3. Flatfoot (Flat Feet)
4. Aggressive Periodontitis (Periodontosis)
5. Palmoplantar Keratoderma (Keratosis Palmaris et Plantaris)

Related Drugs and Biologics

1. Cathepsin C