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Neurofibromatosis type 1 - an update.
Seminars in Pediatric NeurologyNeurofibromatosis type 1 (NF1) is one of the most common genetic conditions. It can be inherited in an autosomal dominant manner, but almost half of cases occur de novo.
Manikum Moodley, Karla Robles Lopez
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Pruritus in neurofibromatosis type 1
Italian Journal of Dermatology and Venereology, 2018 Pruritus in neurofibromatosis type ...
Miraglia, Emanuele +2 more
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Von Recklinghausen's neurofibromatosis: neurofibromatosis type 1
Lancet, The, 2003Rebecca M Reynolds, I W Campbell
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Biochimica et Biophysica Acta (BBA) - Reviews on Cancer, 2000
Neurofibromatosis 1 (NF1) is an autosomal dominant neurocutaneous disorder with an incidence of approximately 1 in 4000. Cognitive deficits and academic learning difficulties are the most common neurological 'complication' of NF1 in childhood and can be responsible for significant lifetime morbidity.
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Neurofibromatosis 1 (NF1) is an autosomal dominant neurocutaneous disorder with an incidence of approximately 1 in 4000. Cognitive deficits and academic learning difficulties are the most common neurological 'complication' of NF1 in childhood and can be responsible for significant lifetime morbidity.
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Neurofibromatosis Type 1: New Developments in Genetics and Treatment.
Journal of American Academy of Dermatology, 2020Neurofibromatosis type 1 is the most common neurocutaneous syndrome with a frequency of 1 in 2500 persons. Diagnosis is paramount in the pretumor stage in order to provide proper anticipatory guidance for a number of neoplasms, both benign and malignant.
B. Wilson +3 more
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Neurofibromatosis type 1 and pregnancy
American Journal of Medical Genetics, 1996Neurofibromatosis Type 1 (NF-1) is an autosomal dominant condition which has markedly variable clinical expression, with manifestations ranging from mild cutaneous lesions to severe orthopedic complications and functional impairment. The current obstetrical literature indicates that women with NF-1 have increased complications associated with pregnancy.
L, Dugoff, E, Sujansky
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Pathophysiology of Neurofibromatosis Type 1
Annals of Internal Medicine, 2006Neurofibromatoses are inherited disorders, designated as neurofibromatosis type 1 (NF1), neurofibromatosis type 2, and schwannomatosis, that tend to result in benign tumors of the nerve sheath.
Amy, Theos, Bruce R, Korf
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2015
Neurofibromatosis type 1 (NF1), previously known as von Recklinghausen disease, is a neurogenetic disorder distinct from neurofibromatosis type 2 (NF2). Approximately 1:2500 to 1:3500 individuals worldwide are affected, regardless of ethnicity or race.
Jacqueline L, Anderson, David H, Gutmann
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Neurofibromatosis type 1 (NF1), previously known as von Recklinghausen disease, is a neurogenetic disorder distinct from neurofibromatosis type 2 (NF2). Approximately 1:2500 to 1:3500 individuals worldwide are affected, regardless of ethnicity or race.
Jacqueline L, Anderson, David H, Gutmann
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The Diagnosis and Management of Neurofibromatosis Type 1.
The Medical clinics of North America, 2019Neurofibromatosis type 1 (NF1), NF2, and schwannomatosis are related, but distinct, tumor suppressor syndromes characterized by a predilection for tumors in the central and peripheral nervous systems.
K. I. Ly, Jaishri O. Blakeley
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Treatment of Neurofibromatosis Type 1
Current Treatment Options in Neurology, 2015Neurofibromatosis type 1 (NF1) is a genetic multisystemic disorder involving the skin, the central and peripheral nervous systems, bones, and the cardiovascular and endocrine systems. This condition is caused by inherited or de novo mutations of the NF1 gene at the 17q11.2 chromosomal region, a gene that codes for the protein neurofibromin ...
C. Sabatini +4 more
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