The Comprehensive NF Center @ NYU presents:
Neurofibroma Educational Series: Neurofibromatosis type 2: an update

CART Transcript - Can be found Here

Event Information

Date: Tuesday, January 31, 2012
Presenter: John G. Pappas, MD
Title: Director of the NYU Clinical Genetic Services

Description

Neurofibromatosis type 2 is an autosomal dominant genetic condition associated with tumors of the nerve for hearing, and tumors of the membranes around the brain and spinal cord. People with this condition are born with one mutated copy of the NF2 gene in each cell. In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF2 gene and occur in people with no history of the disorder in their family.

This program included descriptions of the clinical features, advances and difficulties in molecular diagnosis, current treatment and controversies, simplified molecular pathways and drug development and the pertinent genetic counseling.

CART Transcript - CART Transcript is now available

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