Neurofibromatosis Type 1
Keyword(s):
Neurofibromatosis type 1 is a common, autosomal dominant, monogenetic neurocutaneous disorder. It is characterized by café au lait spots, axillary and inguinal freckling, Lisch nodules, optic pathway gliomas, neurofibromas, and distinctive bony abnormalities. Also associated with this condition are other central nervous system tumors, scoliosis, hypertension, vascular abnormalities, and cognitive issues such as learning disabilities and attention deficit-hyperactivity disorder.
1993 ◽
Vol 107
(1)
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pp. 6-11
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2006 ◽
Vol 48
(12)
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pp. 973
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2007 ◽
Vol 48
(12)
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pp. 973-977
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2016 ◽
Vol 107
(6)
◽
pp. 465-473
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Keyword(s):
2012 ◽
Vol 158A
(9)
◽
pp. 2225-2232
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