Kindler syndrome: report of two cases and review of the literature.

  title={Kindler syndrome: report of two cases and review of the literature.},
  author={Andrew Forman and Julie S. Prendiville and Nancy B. Esterly and Adelaide Ann Hebert and Madeleine Duvic and Yuji Horiguchi and Jacqueline Fine},
  journal={Pediatric dermatology},
  volume={6 2},
We evaluated two patients with hereditary bullous poikiloderma. Both had acral bullae, generalized poikiloderma with prominent atrophy, and acral keratoses. One patient, with sporadic disease, had, in addition, urethral and subglottic stenoses, webbing of digits, and poor dentition. The other patient, whose disease was dominantly inherited, had koilonychia. The results of cutaneous histopathology, electron microscopy, and immunofluorescence mapping studies are presented. It is possible that… CONTINUE READING


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