Literature DB >> 36262581

KID Syndrome: A Rare Congenital Ichthyosiform Disorder.

U N Raghavon1, Neela V Bhuptani1, Bharti K Patel1.   

Abstract

Entities:  

Year:  2022        PMID： 36262581      PMCID： PMC9574145          DOI： 10.4103/idoj.idoj_651_21

Source DB:  PubMed          Journal:  Indian Dermatol Online J        ISSN： 2229-5178


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  3 in total

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

Authors:  R J Rycroft; E J Moynahan; R S Wells
Journal:  Br J Dermatol       Date:  1976-02       Impact factor: 9.302

2.  The keratitis, ichthyosis, and deafness (KID) syndrome.

Authors:  B A Skinner; M C Greist; A L Norins
Journal:  Arch Dermatol       Date:  1981-05

3.  Keratitis-Ichthyosis-Deafness syndrome: A rare congenital disorder.

Authors:  Vinay Shanker; Mudita Gupta; Aditi Prashar
Journal:  Indian Dermatol Online J       Date:  2012-01
  3 in total

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