| Autor: |
Seirafi H; Department of Dermatology, Razi skin hospital, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran., Khezri S, Morowati S, Kamyabhesari K, Mirzaeipour M, Khezri F |
| Jazyk: |
angličtina |
| Zdroj: |
Dermatology online journal [Dermatol Online J] 2011 Mar 15; Vol. 17 (3), pp. 3. Date of Electronic Publication: 2011 Mar 15. |
| Abstrakt: |
Vohwinkel syndrome (mutilating and diffuse palmoplantar keratoderma) is associated with various extracutaneous features including icthyosis and deafness. Its mode of inheritance is autosomal dominant with mutation in loricrin and Connexin 26 genes. Here we report a mutilating and focal palmoplantar keratoderma in two siblings with congenital hypotrichosis and probably autosomal recessive inheritance that appears to be a new variant of Vohwinkel syndrome. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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