Neurofibromatosis (NF) is a genetically transmitted autosomal dominant disorder with variable penetrance and about 50% of cases representing new mutations. It is progressive in nature and one of its unique feature is the diversity of clinical expression from one patent to another and even within a family. The disease is often characterized by complex and multicellular neurofibroma. It may also lead to different complications throughout the life of an affected individual. We report a case of NF involving alveolus of maxilla and mandible causing expansion of the buccal and lingual cortical plates in a 10-year-old gir
Introduction: Facial plexiform neurofibroma (FPN) is a rare tumor appearing on the face. It involves...
Neurofibroma(NF) is one of the common well known autosomal dominant inheritable entity with a preval...
Neurofibromatosis type 1 (NF1) is a clinically and genetically distinct disease involving both neuro...
Neurofibromatosis type 1 (NF1) is a common genetic disease whose dermatological lesions are at the f...
Abtsract Neurofibromatosis type 1 (NF1) is one of the most common inherited syndromes. The literatur...
Neurofibromatosis designates a group of neurocutaneous disorder that essentially affect the neural t...
Neurofibromatosis type I is one of the most common genetic diseases and it may have oral manifestati...
Background: Neurofibromatosis 1 (NF1) is an autosomal dominant genetic disorder. The expression of N...
The scientific literature is poor of data concerning NF1-related oral manifestations in children. Th...
La neurofibromatosis tipo I (NF1) es una alteración autosómica dominante que se manifiesta con múlti...
Neurofibroma is a benign peripheral nerve sheath tumor, which is one of the most frequent tumors of ...
A case of type 1 neurofibromatosis is presented that illustrates oral manifestations and their role ...
Neurofibromas (NFs) are rare neurogenic tumors of the oral cavity. They can present as solitary, or ...
OBJECTIVE: The aim of this study is to analyse alterations of the tongue and the correlation between...
We describe the case of a patient diagnosed with neurofibromatosis type 1 (NF1) where unusually exte...
Introduction: Facial plexiform neurofibroma (FPN) is a rare tumor appearing on the face. It involves...
Neurofibroma(NF) is one of the common well known autosomal dominant inheritable entity with a preval...
Neurofibromatosis type 1 (NF1) is a clinically and genetically distinct disease involving both neuro...
Neurofibromatosis type 1 (NF1) is a common genetic disease whose dermatological lesions are at the f...
Abtsract Neurofibromatosis type 1 (NF1) is one of the most common inherited syndromes. The literatur...
Neurofibromatosis designates a group of neurocutaneous disorder that essentially affect the neural t...
Neurofibromatosis type I is one of the most common genetic diseases and it may have oral manifestati...
Background: Neurofibromatosis 1 (NF1) is an autosomal dominant genetic disorder. The expression of N...
The scientific literature is poor of data concerning NF1-related oral manifestations in children. Th...
La neurofibromatosis tipo I (NF1) es una alteración autosómica dominante que se manifiesta con múlti...
Neurofibroma is a benign peripheral nerve sheath tumor, which is one of the most frequent tumors of ...
A case of type 1 neurofibromatosis is presented that illustrates oral manifestations and their role ...
Neurofibromas (NFs) are rare neurogenic tumors of the oral cavity. They can present as solitary, or ...
OBJECTIVE: The aim of this study is to analyse alterations of the tongue and the correlation between...
We describe the case of a patient diagnosed with neurofibromatosis type 1 (NF1) where unusually exte...
Introduction: Facial plexiform neurofibroma (FPN) is a rare tumor appearing on the face. It involves...
Neurofibroma(NF) is one of the common well known autosomal dominant inheritable entity with a preval...
Neurofibromatosis type 1 (NF1) is a clinically and genetically distinct disease involving both neuro...