Objectives: To describe the prevalence, demographics and characteristics of a novel radiological entity in neurofibromatosis type 1: diffuse neurofibromatous tissue (DNFT) Design: Aretrospective, descriptive review of MDT and radiology notes. Methods: Of the 1049 patients from the NF1 adult radiology MDT minutes (2009–2021), 77 patients with DNFT were identified and clinical data were collected. MRI scans from 20 DNFT cases were interpreted. Results: Although overall gender distribution of DNFT was roughly even, it was more prevalent in females (73.9%) at the sacroiliac joint—where this entity was most common (29.9%). DNFT often involves the fibrous part of the sacroiliac joint and is seen as diffuse, streaky infiltrating tissues that cause...
A neurofibromatose tipo 1 é uma das enfermidades genéticas mais comuns da espécie humana com padrão ...
Neurofibromatosis 1 (NF1) is a genetic disease characterized by cutaneous, neurological and osseous ...
Neurofibromatosis type 1 is one of the most frequently inherited diseases affecting 1:3500 newborn. ...
Neurofibromatosis type 1 (NF1) or von Recklinghausen disease is one of the most common genetic disea...
This issue of eMedRef provides information to clinicians on the pathophysiology, diagnosis, and ther...
Dural ectasia denotes circumferential expansion or dilatation of the dural sac, and has been frequen...
Neurofibromatosis type 1 (NF1) or Von Recklinghausen's disease is a dominantly inherited genetic, mu...
Neurofibromatosis (NF-1), know as Von Recklinghausen's disease, is one of the most common genetic di...
Neurofibromatosis Type 1 (NF1) is a common autosomal dominant disorder characterized by high penetra...
Introduction: Neurofibromatosis includes a group of genetic diseases that cause tumors affecting ner...
Neurofibromatosis type 1 (NF1) is characterized by major and minor cutaneous findings, whose recogni...
Neurofibromatosis Type 1 (NF1) is a common autosomal dominant disorder characterized by high penetra...
Neurofibromatosis type 1 (NF1) is characterized by major and minor cutaneous findings, whose recogni...
Introduction: Gliomas in the brain and the optic pathway affect up to 20% of all children with neuro...
SUMMARY • Type 1 neurofibromatosis is a phacomatosis inherited as an autosomal dominant disorder. It...
A neurofibromatose tipo 1 é uma das enfermidades genéticas mais comuns da espécie humana com padrão ...
Neurofibromatosis 1 (NF1) is a genetic disease characterized by cutaneous, neurological and osseous ...
Neurofibromatosis type 1 is one of the most frequently inherited diseases affecting 1:3500 newborn. ...
Neurofibromatosis type 1 (NF1) or von Recklinghausen disease is one of the most common genetic disea...
This issue of eMedRef provides information to clinicians on the pathophysiology, diagnosis, and ther...
Dural ectasia denotes circumferential expansion or dilatation of the dural sac, and has been frequen...
Neurofibromatosis type 1 (NF1) or Von Recklinghausen's disease is a dominantly inherited genetic, mu...
Neurofibromatosis (NF-1), know as Von Recklinghausen's disease, is one of the most common genetic di...
Neurofibromatosis Type 1 (NF1) is a common autosomal dominant disorder characterized by high penetra...
Introduction: Neurofibromatosis includes a group of genetic diseases that cause tumors affecting ner...
Neurofibromatosis type 1 (NF1) is characterized by major and minor cutaneous findings, whose recogni...
Neurofibromatosis Type 1 (NF1) is a common autosomal dominant disorder characterized by high penetra...
Neurofibromatosis type 1 (NF1) is characterized by major and minor cutaneous findings, whose recogni...
Introduction: Gliomas in the brain and the optic pathway affect up to 20% of all children with neuro...
SUMMARY • Type 1 neurofibromatosis is a phacomatosis inherited as an autosomal dominant disorder. It...
A neurofibromatose tipo 1 é uma das enfermidades genéticas mais comuns da espécie humana com padrão ...
Neurofibromatosis 1 (NF1) is a genetic disease characterized by cutaneous, neurological and osseous ...
Neurofibromatosis type 1 is one of the most frequently inherited diseases affecting 1:3500 newborn. ...