| KID syndrome associated with features of ichthyosis hystrix. | |
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MedLine Citation:
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PMID: 10792799 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Keratitis-ichthyosis-deafness (KID) syndrome is a congenital ectodermal disorder causing erythrokeratoderma, vascularizing keratitis, and neurosensory deafness. Ichthyosis hystrix is a rare cutaneous disease characterized by well-demarcated, spiky, verrucous, linear plaques that is believed to be a clinical and pathologic chimera of two autosomal dominant diseases: epidermal nevus and epidermolytic hyperkeratosis. We present a patient with the classic triad of KID syndrome with clinical and histologic features of ichthyosis hystrix. This case demonstrates that KID syndrome comprises a spectrum of ectodermal disorders which may include diseases such as hystrix ichthyosis and deafness (HID) syndrome. |
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Authors:
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H C Nousari; A Kimyai-Asadi; J L Pinto |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Pediatric dermatology Volume: 17 ISSN: 0736-8046 ISO Abbreviation: Pediatr Dermatol Publication Date: 2000 Mar-Apr |
Date Detail:
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Created Date: 2000-07-13 Completed Date: 2000-07-13 Revised Date: 2009-03-03 |
Medline Journal Info:
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Nlm Unique ID: 8406799 Medline TA: Pediatr Dermatol Country: UNITED STATES |
Other Details:
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Languages: eng Pagination: 115-7 Citation Subset: IM |
Affiliation:
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Department of Dermatology, Johns Hopkins Medical Institutions, Baltimore, Maryland 21205, USA. hnousari@welchlink.welch.jhu.edu |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Argentina Biopsy, Needle Child Deafness* Humans Ichthyosis Vulgaris / diagnosis*, pathology Keratitis / diagnosis* Male Prognosis Syndrome |
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