Clinical and genetic aspects of neurofibromatosis 1.

Volume: 12, Issue: 1, Pages: 1 - 11
Published: Jan 1, 2010
Abstract
Neurofibromatosis 1 is an autosomal dominant disorder characterized by multiple cafe-au-lait spots, axillary and inguinal freckling, multiple cutaneous neurofibromas, and iris Lisch nodules. Learning disabilities are present in at least 50% of individuals with neurofibromatosis 1. Less common but potentially more serious manifestations include plexiform neurofibromas, optic nerve and other central nervous system gliomas, malignant peripheral...
Paper Details
Title
Clinical and genetic aspects of neurofibromatosis 1.
Published Date
Jan 1, 2010
Volume
12
Issue
1
Pages
1 - 11
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