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Mutation-Proved Clouston Syndrome in a Large Indian Family with a Variant Phenotype.
Khatter, Sangeeta; Puri, Ratna Dua; Mahay, Sunita Bijarnia; Bhai, Pratibha; Saxena, Renu; Verma, Ishwar C.
Afiliación
  • Khatter S; Department of Medical Genetics, Institute of Genomics and Medical Genetics, Sir Ganga Ram Hospital, New Delhi, India.
  • Puri RD; Department of Medical Genetics, Institute of Genomics and Medical Genetics, Sir Ganga Ram Hospital, New Delhi, India.
  • Mahay SB; Department of Medical Genetics, Institute of Genomics and Medical Genetics, Sir Ganga Ram Hospital, New Delhi, India.
  • Bhai P; Department of Medical Genetics, Institute of Genomics and Medical Genetics, Sir Ganga Ram Hospital, New Delhi, India.
  • Saxena R; Department of Medical Genetics, Institute of Genomics and Medical Genetics, Sir Ganga Ram Hospital, New Delhi, India.
  • Verma IC; Department of Medical Genetics, Institute of Genomics and Medical Genetics, Sir Ganga Ram Hospital, New Delhi, India.
Indian J Dermatol ; 64(2): 143-145, 2019.
Article en En | MEDLINE | ID: mdl-30983611
Hereditary ectodermal dysplasias, a group of disorders affecting skin, hair, nails, and teeth, consist of two main clinical forms - hypohidrotic and hidrotic. Clouston syndrome is a hidrotic ectodermal dysplasia characterized by a triad of generalized hypotrichosis, palmoplantar hyperkeratosis, and nail dystrophy. This paper reports a large Indian family with Clouston syndrome but with the absence of palmoplantar keratoderma, one of the features of the typical triad, thus representing phenotypic heterogeneity, in spite of the presence of a common known mutation in GJB6 gene (p.Gly11Arg).
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Indian J Dermatol Año: 2019 Tipo del documento: Article País de afiliación: India

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Indian J Dermatol Año: 2019 Tipo del documento: Article País de afiliación: India