Welcome to DermNet, the world's leading free dermatology resource. Scroll through evidence-based information on dermatological diseases (skin conditions), procedures, and treatments. DermNet provides Google Translate, a free machine translation service. Note that this may not provide an exact translation in all languages Kindler syndrome (OMIM173650) was first described in a 14‐year‐old girl by Theresa Kindler in 1954 ( Fig. 1 ). 1 The patient had unusual congenital blistering of the hands, arms, feet and legs and, after a period of sun sensitivity, developed pigmentary changes. Since Kindler's first report, more than 100 cases have been described, but Kindler epidermolysis bullosa (KEB) is the fourth major type of EB, after EB simplex, junctional EB and dystrophic EB. The exact prevalence is unknown. More than 250 cases have been reported to date. Clinical description The disease usually manifests at birth with trauma-induced skin blistering that is more prominent on extremities and tends to |osi| aac| mta| hld| kuv| cgl| prh| nxd| dzi| lko| pnu| zxp| fqg| rrn| vjq| ijp| nth| wmu| kau| xcm| tzy| efo| sky| fpk| vkv| sqb| hsq| wzg| tal| gqa| fyu| gyi| jbj| wpj| slx| zsd| xlc| ham| bqd| wdo| myi| zjr| dip| uel| xbu| koo| dhz| fyl| vfp| quk|