Literature DB >> 1252351

Atypical ichthyosiform erythrodernam deafness and keratitis. A report of two cases.

R J Rycroft, E J Moynahan, R S Wells.   

Abstract

Two patients with ichthyosiform erythroderma of the same unusual but characteristic distribution are described. Both patients were born with perceptive deafness and developed severe vascularizing keratitis in early childhood. There is no family history of the disorder in either case. This syndrome is discussed in relation to previous reports of atypical ichthyosiform erythroderma associated with deafness.

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Year:  1976        PMID: 1252351     DOI: 10.1111/j.1365-2133.1976.tb04372.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  1 in total

1.  KID Syndrome: A Rare Congenital Ichthyosiform Disorder.

Authors:  U N Raghavon; Neela V Bhuptani; Bharti K Patel
Journal:  Indian Dermatol Online J       Date:  2022-06-24
  1 in total

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