Literature DB >> 12047643

Fatal septicemia in an infant with keratitis, ichthyosis, and deafness (KID) syndrome.

Amy Gilliam1, Mary L Williams.   

Abstract

Keratitis, ichthyosis, and deafness (KID) syndrome is a rare congenital disorder of unknown etiology in which increased susceptibility to viral, bacterial, and mycotic infections has been observed. We report an infant with KID syndrome who died from overwhelming systemic infection. To date, investigations into the immune function of patients with this syndrome have not revealed a common underlying systemic immune deficit. However, the severity of infections and multiplicity of organisms observed in this syndrome suggest that a primary immunodeficiency is present in addition to an impaired cutaneous barrier to microorganisms.

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Year:  2002        PMID: 12047643     DOI: 10.1046/j.1525-1470.2002.00075.x

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  8 in total

1.  Cochleosaccular dysplasia associated with a connexin 26 mutation in keratitis-ichthyosis-deafness syndrome.

Authors:  Andrew J Griffith; Yandan Yang; Shannon P Pryor; Hong-Joon Park; Ethylin Wang Jabs; Joseph B Nadol; Laura J Russell; Daniel I Wasserman; Gabriele Richard; Joe C Adams; Saumil N Merchant
Journal:  Laryngoscope       Date:  2006-08       Impact factor: 3.325

2.  More than keratitis, ichthyosis, and deafness: Multisystem effects of lethal GJB2 mutations.

Authors:  Evelyn Lilly; Christopher G Bunick; Alexander M Maley; Shali Zhang; Mary K Spraker; Amy J Theos; Karina L Vivar; Lucia Seminario-Vidal; Adam E Bennett; Robert Sidbury; Yasushi Ogawa; Masashi Akiyama; Barbara Binder; Smail Hadj-Rabia; Raffaella A Morotti; Earl J Glusac; Keith A Choate; Gabriele Richard; Leonard M Milstone
Journal:  J Am Acad Dermatol       Date:  2018-10-02       Impact factor: 11.527

Review 3.  Connexin channels in congenital skin disorders.

Authors:  Evelyn Lilly; Caterina Sellitto; Leonard M Milstone; Thomas W White
Journal:  Semin Cell Dev Biol       Date:  2016-01-13       Impact factor: 7.727

Review 4.  Cochlear histopathology in human genetic hearing loss: State of the science and future prospects.

Authors:  Krishna Bommakanti; Janani S Iyer; Konstantina M Stankovic
Journal:  Hear Res       Date:  2019-08-19       Impact factor: 3.208

5.  Phenotypic variability in gap junction syndromic skin disorders: experience from KID and Clouston syndromes' clinical diagnostics.

Authors:  Anna Kutkowska-Kaźmierczak; Katarzyna Niepokój; Katarzyna Wertheim-Tysarowska; Aleksandra Giza; Maria Mordasewicz-Goliszewska; Jerzy Bal; Ewa Obersztyn
Journal:  J Appl Genet       Date:  2015-01-10       Impact factor: 3.240

6.  Roles of aberrant hemichannel activities due to mutant connexin26 in the pathogenesis of KID syndrome.

Authors:  T Taki; T Takeichi; K Sugiura; M Akiyama
Journal:  Sci Rep       Date:  2018-08-27       Impact factor: 4.379

7.  Connexin hemichannel inhibition ameliorates epidermal pathology in a mouse model of keratitis ichthyosis deafness syndrome.

Authors:  Caterina Sellitto; Leping Li; Thomas W White
Journal:  Sci Rep       Date:  2021-12-16       Impact factor: 4.379

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

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

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