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Kindler Syndrome — Gene Therapy & Clinical Trials | FollowGene
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Kindler Syndrome
Kindler Syndrome
Prevalence:
1/1000000
dermatologic
Official
·
OMIM:173650
Official
·
ORPHA2908
Skin fragility and photosensitivity due to FERMT1 gene mutations.
Associated Genes
FERMT1
FERM Domain Containing Kindlin 1
Chromosome 20
Autosomal Recessive