Volume : VII, Issue : II, February - 2017

STURGE WEBER SYNDROME: CASE REPORT AND REVIEW

Jay Sanghavi, Marmik Patel, J D Lakhani, Santosh Kumar

Abstract :

 Sturge–Weber Syndrome (encephelo–trigeminal angiomatosis) is a congenital, rare disorder characterized by a facial birthmark and neurological abnormalities. It  is a developmental capillary vascular disorder originating during emyogenesis before neural crest migration, from errors in development of ectoderm and mesoderm in the anterior neural primordium due possibly to somatic mutations. ¹

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Article: Download PDF   DOI : 10.36106/ijar  

Cite This Article:

Jay Sanghavi, Marmik Patel, J D Lakhani, Santosh Kumar, STURGE WEBER SYNDROME: CASE REPORT AND REVIEW, INDIAN JOURNAL OF APPLIED RESEARCH : Volume‾7 | Issue‾2 | February‾2017

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