PurposeNeurofibromatosis type I (NF-I) is an autosomal dominant disorder affecting one in 3000 individuals. Vascular abnormalities are a well-recognized manifestation of NF-I. The purpose of this study is to review the spectrum, management, and clinical outcome of patients with vascular abnormalities and NF-I.MethodsWe retrospectively reviewed 31 patients (15 males, 16 females) with clinical NF-I and vascular abnormalities identified from imaging or operative findings between 1976 and 2005.ResultsThe diagnosis of NF-I was made at a mean age of 11 ± 10 years with vascular lesions identified at a mean age of 38 ± 16 years. There were 76 vascular abnormalities, including 38 aneurysms, 20 arterial stenoses, 5 arteriovenous malformations (AVM), ...
Background and purpose The aim of the study was to assess anatomical variants and abnormalities in c...
A 38-year-old woman with neurofibromatosis type 1 was referred for massive swelling of the left thig...
Neurofibromatosis (NF) is a common autosomal dominant disease characterized by the development of ha...
PurposeNeurofibromatosis type I (NF-I) is an autosomal dominant disorder affecting one in 3000 indiv...
AbstractIntroductionIntrinsic lesions of the arterial wall are important manifestations of Neurofibr...
Abstract Introduction Intrinsic lesions of the arterial wall are important manifestations of Neurofi...
Background: Neurofibromatosis type 1 (NF1) is a neurocutaneous syndrome, due to heterozygous pathoge...
SUMMARY: Although neurofibromatosis type 1 (NF-1) is commonly considered neurocutaneous, se-vere art...
Neurofibromatosis type 1 (NF1) is a relatively common single-gene disorder, and is caused by heteroz...
Neurofibromatosis type 1 (NF1) is a relatively common single-gene disorder, and is caused by heteroz...
Neurofibromatosis type 1 (NF1) is a relatively common single-gene disorder, and is caused by heteroz...
Subjects with Neurofibromatosis 1 (NF1) develop vascular complications. The protein product of the g...
Subjects with Neurofibromatosis 1 (NF1) develop vascular complications. The protein product of the g...
A 48-year-old woman with neurofibromatosis type 1 (NF1) experienced progressive forearm swelling cou...
Subjects with Neurofibromatosis 1 (NF1) develop vascular complications. The protein product of the g...
Background and purpose The aim of the study was to assess anatomical variants and abnormalities in c...
A 38-year-old woman with neurofibromatosis type 1 was referred for massive swelling of the left thig...
Neurofibromatosis (NF) is a common autosomal dominant disease characterized by the development of ha...
PurposeNeurofibromatosis type I (NF-I) is an autosomal dominant disorder affecting one in 3000 indiv...
AbstractIntroductionIntrinsic lesions of the arterial wall are important manifestations of Neurofibr...
Abstract Introduction Intrinsic lesions of the arterial wall are important manifestations of Neurofi...
Background: Neurofibromatosis type 1 (NF1) is a neurocutaneous syndrome, due to heterozygous pathoge...
SUMMARY: Although neurofibromatosis type 1 (NF-1) is commonly considered neurocutaneous, se-vere art...
Neurofibromatosis type 1 (NF1) is a relatively common single-gene disorder, and is caused by heteroz...
Neurofibromatosis type 1 (NF1) is a relatively common single-gene disorder, and is caused by heteroz...
Neurofibromatosis type 1 (NF1) is a relatively common single-gene disorder, and is caused by heteroz...
Subjects with Neurofibromatosis 1 (NF1) develop vascular complications. The protein product of the g...
Subjects with Neurofibromatosis 1 (NF1) develop vascular complications. The protein product of the g...
A 48-year-old woman with neurofibromatosis type 1 (NF1) experienced progressive forearm swelling cou...
Subjects with Neurofibromatosis 1 (NF1) develop vascular complications. The protein product of the g...
Background and purpose The aim of the study was to assess anatomical variants and abnormalities in c...
A 38-year-old woman with neurofibromatosis type 1 was referred for massive swelling of the left thig...
Neurofibromatosis (NF) is a common autosomal dominant disease characterized by the development of ha...