Literature DB >> 2612042

Polyostotic fibrous dysplasia associated with extensive linear epidermal naevi.

M H Rustin, C B Bunker, J J Gilkes, T W Robinson, P M Dowd.   

Abstract

Albright's syndrome is characterized by the combination of polyostotic fibrous dysplasia, precocious puberty and café-au-lait spots. We describe a patient with polyostotic fibrous dysplasia who also had extensive linear epidermal naevi, an association that has not been previously described in the English literature.

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Year:  1989        PMID: 2612042     DOI: 10.1111/j.1365-2230.1989.tb02589.x

Source DB:  PubMed          Journal:  Clin Exp Dermatol        ISSN: 0307-6938            Impact factor:   3.470


  4 in total

1.  Another epidermal naevus with polyostotic anomalies?

Authors:  Ahmad I Alomari
Journal:  Ann R Coll Surg Engl       Date:  2011-01       Impact factor: 1.891

Review 2.  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

3.  Epidermal naevus syndrome associated with polyostotic fibrous dysplasia and central precocious puberty.

Authors:  A C Yu; V Ng; C Dicks-Mireaux; D B Grant
Journal:  Eur J Pediatr       Date:  1995-02       Impact factor: 3.183

Review 4.  DIAGNOSIS OF ENDOCRINE DISEASE: Mosaic disorders of FGF23 excess: Fibrous dysplasia/McCune-Albright syndrome and cutaneous skeletal hypophosphatemia syndrome.

Authors:  Luis F de Castro; Diana Ovejero; Alison M Boyce
Journal:  Eur J Endocrinol       Date:  2020-05       Impact factor: 6.664

  4 in total

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