Striate palmoplantar keratoderma is an isolated, focal, hereditary palmoplantar keratoderma characterized by linear hyperkeratosis along the flexor aspect of the fingers and on palms, as well as focal hyperkeratosis of the plantar skin. Patients present with painful thickening of the skin on palms and soles, with occasional fissuring, blistering and hyperhidrosis. Rarely, hyperkeratosis on other areas may be seen (knees, dorsal aspects of the digits). Histopatologically, widened intercellular spaces between keratinocytes are observed. [ Orphanet:50942 ]
Synonyms: keratosis palmoplantaris striata keratosis palmoplantaris varians of Wachters keratosis palmoplantaris striata et areata
Term information
- MEDGEN:1631598 (MONDO:equivalentTo)
- Orphanet:50942 (MONDO:equivalentTo)
- UMLS:C4707237 (MONDO:equivalentTo)
- DOID:0081105 (MONDO:equivalentTo)
- GARD:15016 (MONDO:GARD)
- SCTID:764958008 (MONDO:equivalentTo)
ordo_disorder, gard_rare, otar, rare, nord_rare, orphanet_rare
https://github.com/monarch-initiative/mondo/issues/6749
https://github.com/monarch-initiative/mondo/issues/6877
http://linkedlifedata.com/resource/umls/id/C4707237
http://purl.obolibrary.org/obo/DOID_0081105
http://identifiers.org/snomedct/764958008
http://www.orpha.net/ORDO/Orphanet_50942
http://identifiers.org/medgen/1631598