Literature DB >> 34760092

A non-classic form of McCune Albright syndrome with different presentations and review of the literatures.

Alireza Navabazam1, Fatemeh Owlia2, Mohammad Hassan Akhavan Karbassi2, Roqayeh Hakimian3.   

Abstract

BACKGROUND: McCune Albright syndrome (MAS) is a rare heterogeneous clinical syndrome without any predilection for ethnic group. Classic form includes triad of fibrous dysplasia, café au late spots and autonomous hyper function of one or more endocrine pathways. CASE REPORT: We report the case of an 18-year old girl with non-classic form of MAS .New aspect of this case report attributed to multiple sebaceous adenoma.
CONCLUSION: The new finding of our case of MAS was not reported before. Periodic follow-up with different radiologic and laboratory tests should be considered after suspicion to MAS.

Entities:  

Keywords:  Cafe-au-Lait spots; Fibrous dysplasia; Polyostotic; Precocious; Puberty

Year:  2021        PMID: 34760092      PMCID: PMC8559639          DOI: 10.22088/cjim.12.0.401

Source DB:  PubMed          Journal:  Caspian J Intern Med        ISSN: 2008-6164


  5 in total

1.  McCune-Albright syndrome: a case report in a male.

Authors:  Krina B Patel
Journal:  Indian J Dermatol Venereol Leprol       Date:  2010 Nov-Dec       Impact factor: 2.545

Review 2.  McCune-Albright syndrome: clinical picture and natural history in children and adolescents.

Authors:  Thomas M K Völkl; Helmuth G Dörr
Journal:  J Pediatr Endocrinol Metab       Date:  2006-05       Impact factor: 1.634

Review 3.  McCune-Albright syndrome: growth hormone and prolactin hypersecretion.

Authors:  Athanasios Christoforidis; Ilianna Maniadaki; Richard Stanhope
Journal:  J Pediatr Endocrinol Metab       Date:  2006-05       Impact factor: 1.634

4.  Neonatal McCune-Albright syndrome with systemic involvement: a case report.

Authors:  Rita Lourenço; Patrícia Dias; Raquel Gouveia; Ana Berta Sousa; Graça Oliveira
Journal:  J Med Case Rep       Date:  2015-09-04

5.  Craniofacial polyostotic fibrous dysplasia: A rare case.

Authors:  Fatemeh Owlia; Mohammad-Hassan Akhavan Karbassi
Journal:  Dent Res J (Isfahan)       Date:  2014-07
  5 in total

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