Visual impairment reversal with oral acitretin therapy in keratitis-ichthyosis-deafness (KID) syndrome

نویسندگان

  • Christopher M. Wolfe
  • Alexander Davis
  • Tarek S. Shaath
  • George F. Cohen
چکیده

GJB2: gap junction protein b2 KID: keratitis-ichthyosis-deafness INTRODUCTION Keratitis-ichthyosis-deafness (KID) syndrome is a rare genodermatosis with approximately 100 published cases. Although it is classified as an autosomal dominant disorder, more than 90% of cases are caused by sporadic mutations predominantly in gap junction protein b2 (GJB2) on chromosome 13q11-q12 (OMIM 148210). GJB2 encodes connexin 26, a gap junction protein, which plays a role in epithelial differentiation. The characteristic clinical triad includes bilateral sensorineural hearing loss, vascularizing keratitis, and erythrokeratoderma. Treatment with acitretin is reported to clear hyperkeratotic ichthyotic lesions with little effect on vision and hearing.

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منابع مشابه

Connexin 26 (GJB2) mutations in two Swedish patients with atypical Vohwinkel (mutilating keratoderma plus deafness) and KID syndrome both extensively treated with acitretin.

Neuroectodermal syndromes involving the skin and inner ear may be associated with mutations in connexin proteins, which form gap junctions important for intercellular communication. Vohwinkel syndrome (keratodermia mutilans with hearing loss) and keratitis-ichthyosis-deafness (KID) syndrome are rare ectodermal dysplasias associated with dominant mutations in the GJB2 gene encoding connexin 26. ...

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عنوان ژورنال:

دوره 3  شماره 

صفحات  -

تاریخ انتشار 2017