Kindler syndrome: A case presenting with blistering poikiloderma and photosensitivity
Kindler syndrome: A case presenting with blistering poikiloderma and photosensitivity
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Publisher
Medknow Publications Pvt Ltd
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Language
English
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Publisher
Medknow Publications Pvt Ltd
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Contents
Kindler syndrome is a rare genodermatosis with autosomal recessive inheritance and less than 150 cases reported worldwide. It results from loss of function mutation in the KIND1 gene (FERMT1), which has been localized to the short arm of chromosome 20. Onset is just after birth with traumatic blistering healing without scarring, skin fragility, pro...
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Full title
Kindler syndrome: A case presenting with blistering poikiloderma and photosensitivity
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TN_cdi_gale_infotracmisc_A367829162
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A367829162
Other Identifiers
ISSN
2319-7250
DOI
10.4103/2319-7250.131842
