Literature DB >> 21079331

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

Krina B Patel1.   

Abstract

McCune-Albright syndrome (MAS) is a rare, heterogenous, clinical condition caused by a rare genetic mutation. The disorder is more common in females and is characterized by a triad of cutaneous, bone and endocrine abnormalities. We describe a male patient with MAS having multiple café-au-lait macules and deforming polyostotic fibrous dysplasia involving long bones of the limbs, skull and spine without any endocrine abnormality. Severe bone deformities involving almost all bones have not been described previously and this prompted us to present the current case.

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Year:  2010        PMID: 21079331     DOI: 10.4103/0378-6323.72473

Source DB:  PubMed          Journal:  Indian J Dermatol Venereol Leprol        ISSN: 0378-6323            Impact factor:   2.545


  3 in total

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

Authors:  Alireza Navabazam; Fatemeh Owlia; Mohammad Hassan Akhavan Karbassi; Roqayeh Hakimian
Journal:  Caspian J Intern Med       Date:  2021

2.  A Clinical Perspective on Advanced Developments in Bone Biopsy Assessment in Rare Bone Disorders.

Authors:  Sanne Treurniet; Elisabeth M W Eekhoff; Felix N Schmidt; Dimitra Micha; Björn Busse; Nathalie Bravenboer
Journal:  Front Endocrinol (Lausanne)       Date:  2020-06-23       Impact factor: 5.555

3.  McCune-Albright syndrome mimicking malignancy: an endocrine disease from oncologist's perspective.

Authors:  D Bahar Genç; M Alp Özkan; Atilla Büyükgebiz
Journal:  J Clin Res Pediatr Endocrinol       Date:  2012-09
  3 in total

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