Literature DB >> 8010352

Vohwinkel syndrome (mutilating keratoderma) associated with craniofacial anomalies.

A Sensi1, V Bettoli, M R Zampino, E Gandini, E Calzolari.   

Abstract

We describe a female patient with Vohwinkel syndrome (mutilating palmoplantar keratoderma), who in addition showed cleft lip and palate, microcephaly, facial asymmetry, and other anomalies.

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Year:  1994        PMID: 8010352     DOI: 10.1002/ajmg.1320500212

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  3 in total

1.  [Vohwinkel syndrome. Hearing loss and keratoderma on the hands and feet].

Authors:  S Dippold; F Butsch; R Schopf; A Keilmann
Journal:  HNO       Date:  2013-07       Impact factor: 1.284

Review 2.  Hereditary Hearing Impairment with Cutaneous Abnormalities.

Authors:  Tung-Lin Lee; Pei-Hsuan Lin; Pei-Lung Chen; Jin-Bon Hong; Chen-Chi Wu
Journal:  Genes (Basel)       Date:  2020-12-30       Impact factor: 4.096

Review 3.  Diagnosis and Management of Inherited Palmoplantar Keratodermas.

Authors:  Bjorn R Thomas; Edel A O'Toole
Journal:  Acta Derm Venereol       Date:  2020-03-25       Impact factor: 3.875

  3 in total

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