Senter Syndrome (Keratitis-Ichthyosis-Deafness
Syndrome; KID Syndrome; Ichthyosiform
Erythroderma, Corneal Involvement, and Deafness 414c27e 414c27e 414c27e
General: Autosomal recessive.
Ocular: Corneal involvement.
Clinical: Ichthyosiform erythroderma; deafness; hepatomegaly; hepatic cirrhosis; glycogen storage; short stature; mental retardation; hepatitis.
McKusick VA. Mendelian Inheritance in Man; A Catalog of Human Genes and Genetic Disorders, 12th ed. Baltimore: The Johns Hopkins University Press, 1998.
Online Mendelian Inheritance in Man, OMIM. McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University and National Center for Biotechnology Information, National Library of Medicine, February 12, 2007. World Wide Web URL: https://www.ncbi.nlm.nih.gov/omim/.
Senter TP, et al. Atypical ichthyosiform erythroderma and congenital neurosensory deafness-a distinct syndrome. J Pediatr 1978; 92:68-72.
Wilson GN, et al. Keratitis, hepatitis, ichthyosis, and deafness: report and review of KID syndrome. Am J Med Genet 1991; 40:255-259.
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