Volume : VI, Issue : VII, July - 2017

MODIFIED MANAGEMENT IN THE TREATMENT OF CRANIOFACIAL FIBROUS DYSPLASIA: A CASE REPORT

Dr. Laxman Roy Chittaluri, Dr. Ravichandra Ravi

Abstract :

 Fious dysplasia (FD) of  bone is a genetic, non–inherited disease caused by activating mutations of the GNAS1 gene which encodes the α–subunit of the stimulatory G–protein Gs. It may present as an isolated skeletal lesion (monostotic form) or involve multiple skeletal sites (polyostotic form) in addition to single or multiple endocrinoapthies.1 McCune–Alight syndrome (MAS) is a condition which includes a classical triad of polyostotic fious dysplasia, Café au lait macules  and endocrinopathies.2  Whereas, Mazaaud syndrome is the term used to note the combination of FD of bone with myxomas of the skeletal muscle.1

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Article: Download PDF   DOI : 10.36106/ijsr  

Cite This Article:

Dr.laxman roy Chittaluri, Dr. Ravichandra Ravi, MODIFIED MANAGEMENT IN THE TREATMENT OF CRANIOFACIAL FIBROUS DYSPLASIA: A CASE REPORT, INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH : VOLUME-6 | ISSUE-7 | JULY-2017


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