Autor:	Criton S, Vincent Johny
Rok vydání:	2010
Předmět:	Keratitis genetic structures integumentary system otorhinolaryngologic diseases lcsh:Dermatology Ichthyosis sense organs Deafness lcsh:RL1-803 eye diseases
Zdroj:	Indian Journal of Dermatology, Venereology and Leprology, Vol 61, Iss 5, Pp 312-313 (1995)
ISSN:	0378-6323
Popis:	Keratitis, ichthyosis, deafness (KID) syndrome is a genetically determined disorder. The present case is having marked photophobia, bilateral corneal ulceration with vascularisation, neurosensory deafness and skin changes.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::dff05411d3a248fe25bf30f9835e7e23 https://pubmed.ncbi.nlm.nih.gov/20953002 Zobrazit plný text záznamu