Keratitis – ichthyosis – deafness syndrome (Q68337): Difference between revisions
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Síndrome de ceratite (tipo hystrix)-ictiose-surdez (KID/HID) é um transtorno ectodérmico congênito raro caracterizado por ceratite vascularizante, lesões cutâneas hiperceratóticas e perda auditiva. | |||
| description / en | description / en | ||
Keratitis (and hystrix-like) ichthyosis deafness (KID/HID) syndrome is a rare congenital ectodermal disorder characterised by vascularizing keratitis, hyperkeratotic skin lesions and hearing loss. | |||
Revision as of 16:13, 14 August 2026
Keratitis (and hystrix-like) ichthyosis deafness (KID/HID) syndrome is a rare congenital ectodermal disorder characterised by vascularizing keratitis, hyperkeratotic skin lesions and hearing loss.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1152535279 |
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| English | Keratitis – ichthyosis – deafness syndrome |
Keratitis (and hystrix-like) ichthyosis deafness (KID/HID) syndrome is a rare congenital ectodermal disorder characterised by vascularizing keratitis, hyperkeratotic skin lesions and hearing loss. |
