WOS: 000341414400017PubMed ID: 24217084Neurofibromatosis (NF) is a disorder with a wide spectrum of clinical manifestations. Here, we describe a 16-year-old boy with NF1 who had pseudoarthrosis of the 4th and 5th fingers of the left hand. He had specific cutaneous lesions and Lisch nodules in the iris. Because NF1 affects multiple organ systems, patients are likely to benefit most from a multidisciplinary treatment strategy
Introduction. This is the case of a young male patient who presented to his family physician with at...
Neurofibromatosis type 1 (NF1) is an autosomal dominant inherited disorder caused by mutations of ch...
Pachydermoperiostosis (PDP), otherwise known as primary hypertrophic osteoarthropathy, is characteri...
Neurofibromatosis (NF) is a genetic disease leading pathological findings in skin, soft tissue, bone...
We present a 21 year old boy with Neurofibromatosis (NF 1-GROUP 1) affecting the craniofacial region...
Neurofibromatosis (NF-1), know as Von Recklinghausen's disease, is one of the most common genetic di...
INTRODUCTION: Neurofibromatosis Type 1 (NF1) or Von Recklinghausen’s disease, is a rare genetic di...
Abstract: 1Neurofibromatosis (NF) is a group of genetic disorders: NF1, NF2 and schwannomatosis (shw...
Neurofibromatosis type 1 (NF1) or Von Recklinghausen's disease is a dominantly inherited genetic, mu...
Neurofibromatosis-1 (NF1) is one of the most common hereditary multisystemic disorders. The disease ...
Neurofibromatosis type I is an autosomal dominant genetic disorder with an incidence of about 1 in 3...
Objective: Neurofibromatosis type 1 (NF1) is an autosomal dominant tumor predisposition syndrome wit...
Neurofibromatosis (NF) is a term that has been applied to a variety of related syndromes, characteri...
Congenital pseudoarthrosis (CPT) of the tibia is rare congenital anomaly occurring 1 in 190,000 live...
Introduction: Neurofibromatosis includes a group of genetic diseases that cause tumors affecting ner...
Introduction. This is the case of a young male patient who presented to his family physician with at...
Neurofibromatosis type 1 (NF1) is an autosomal dominant inherited disorder caused by mutations of ch...
Pachydermoperiostosis (PDP), otherwise known as primary hypertrophic osteoarthropathy, is characteri...
Neurofibromatosis (NF) is a genetic disease leading pathological findings in skin, soft tissue, bone...
We present a 21 year old boy with Neurofibromatosis (NF 1-GROUP 1) affecting the craniofacial region...
Neurofibromatosis (NF-1), know as Von Recklinghausen's disease, is one of the most common genetic di...
INTRODUCTION: Neurofibromatosis Type 1 (NF1) or Von Recklinghausen’s disease, is a rare genetic di...
Abstract: 1Neurofibromatosis (NF) is a group of genetic disorders: NF1, NF2 and schwannomatosis (shw...
Neurofibromatosis type 1 (NF1) or Von Recklinghausen's disease is a dominantly inherited genetic, mu...
Neurofibromatosis-1 (NF1) is one of the most common hereditary multisystemic disorders. The disease ...
Neurofibromatosis type I is an autosomal dominant genetic disorder with an incidence of about 1 in 3...
Objective: Neurofibromatosis type 1 (NF1) is an autosomal dominant tumor predisposition syndrome wit...
Neurofibromatosis (NF) is a term that has been applied to a variety of related syndromes, characteri...
Congenital pseudoarthrosis (CPT) of the tibia is rare congenital anomaly occurring 1 in 190,000 live...
Introduction: Neurofibromatosis includes a group of genetic diseases that cause tumors affecting ner...
Introduction. This is the case of a young male patient who presented to his family physician with at...
Neurofibromatosis type 1 (NF1) is an autosomal dominant inherited disorder caused by mutations of ch...
Pachydermoperiostosis (PDP), otherwise known as primary hypertrophic osteoarthropathy, is characteri...