Literature DB >> 23745233

Phacomatosis pigmentokeratotica--a patient with hypophosphatemic rickets.

Orlando Oliveira de Morais1, Lidiane Oliveira Costa, Dayane Higa Shinzato, Nayara de Castro Wiziack, Günter Hans-Filho.   

Abstract

The epidermal naevus syndrome (ENS) is a sporadic condition characterized by congenital epidermal naevi associated with anomalies in other organ systems, most commonly the central nervous system and skeleton. We report a case of ENS presenting hypophosphataemic rickets resistant to traditional therapeutic agents.

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Year:  2013        PMID: 23745233

Source DB:  PubMed          Journal:  Skinmed        ISSN: 1540-9740


  1 in total

Review 1.  Cutaneous skeletal hypophosphatemia syndrome: clinical spectrum, natural history, and treatment.

Authors:  D Ovejero; Y H Lim; A M Boyce; R I Gafni; E McCarthy; T A Nguyen; L F Eichenfield; C M C DeKlotz; L C Guthrie; L L Tosi; P S Thornton; K A Choate; M T Collins
Journal:  Osteoporos Int       Date:  2016-08-06       Impact factor: 4.507

  1 in total

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