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ichthyosis hystrix-like with deafness syndrome (HID syndrome)
Pathology:
- keratinizing disorder
- sensorineural deafness
- spiky hyperkeratosis affecting the entire skin
Genetics:
- autosomal-dominant
- associated with defects in GJB2
Clinical manifestations:
- HID syndrome differa from the similar KID syndrome in the extent & time of occurrence of skin symptoms & the severity of the associated keratitis
Related
ichthyosis hystrix-like with deafness syndrome (HID syndrome)
General
genetic syndrome (multisystem disorder)
Database Correlations
OMIM 602540
References
OMIM :accession 602540