Neurofibromatosis (NF), one of the commonest phakomatoses, is characterized by varied clinical manifestations. Segmental NF is one of the uncommon subtypes of NF. We report a young adult presenting with asymptomatic skin lesions- neurofibromas and café-au-lait macules- over localized areas of the lower back, affecting more than one segment. None of the family members were found to have features of segmental NF. Segmental NF may be misdiagnosed as a birthmark or remain undiagnosed for long periods of time, as the patients are often asymptomatic. Moreover, the clinical features are highly variable and range from a small area of skin involvement to involvement over the entire half of the body. This variation is explained by the fact that segme...
A 2-year-old male child born of third degree consanguineous marriage was brought to dermatology outp...
Neurofibromatosis type1 (NF1) with the incidence of 1 in 3500 births, is the most common disorder wh...
Neurofibromatosis type 1 (NF1) is a rare genetic disorder, characterized by the development of benig...
Neurofibromatosis (NF), one of the commonest phakomatoses, is characterized by varied clinical manif...
Neurofibromatosis is a genetic disorder of neural crest-derived cells that primarily affect growth o...
Segmental neurofibromatosis is characterised by a limited, segmental distribution of cutaneous neuro...
Abstract Neurofibromatosis is extremely variable in its presentation. Segmental neurofibromatosis (S...
Two cases of segmental neurofibromatosis (SNF) in a 57-year old woman and in a 52-year old man are r...
Neurofibromatosis (NF) is a genetic disease leading pathological findings in skin, soft tissue, bone...
A 71-year-old woman presented with multiple, flesh-colored, papular lesions on the left dorsal side ...
Objective: Neurofibromatosis (NF) is one of the most commonly seen autosomal dominantly inherited ne...
BackgroundSegmental neurofibromatosis, referred to as mosaic neurofibromatosis 1, patients present w...
BACKGROUND: Neurofibromatosis type 1 (NF-1) is an autsomal dominant disorder which can occasionally...
Neurofibromatosis-1 (NF1) is one of the most common hereditary multisystemic disorders. The disease ...
Neurofibromatosis type 1 (NF1) is a neurocutaneous condition with an autosomal dominant pattern of i...
A 2-year-old male child born of third degree consanguineous marriage was brought to dermatology outp...
Neurofibromatosis type1 (NF1) with the incidence of 1 in 3500 births, is the most common disorder wh...
Neurofibromatosis type 1 (NF1) is a rare genetic disorder, characterized by the development of benig...
Neurofibromatosis (NF), one of the commonest phakomatoses, is characterized by varied clinical manif...
Neurofibromatosis is a genetic disorder of neural crest-derived cells that primarily affect growth o...
Segmental neurofibromatosis is characterised by a limited, segmental distribution of cutaneous neuro...
Abstract Neurofibromatosis is extremely variable in its presentation. Segmental neurofibromatosis (S...
Two cases of segmental neurofibromatosis (SNF) in a 57-year old woman and in a 52-year old man are r...
Neurofibromatosis (NF) is a genetic disease leading pathological findings in skin, soft tissue, bone...
A 71-year-old woman presented with multiple, flesh-colored, papular lesions on the left dorsal side ...
Objective: Neurofibromatosis (NF) is one of the most commonly seen autosomal dominantly inherited ne...
BackgroundSegmental neurofibromatosis, referred to as mosaic neurofibromatosis 1, patients present w...
BACKGROUND: Neurofibromatosis type 1 (NF-1) is an autsomal dominant disorder which can occasionally...
Neurofibromatosis-1 (NF1) is one of the most common hereditary multisystemic disorders. The disease ...
Neurofibromatosis type 1 (NF1) is a neurocutaneous condition with an autosomal dominant pattern of i...
A 2-year-old male child born of third degree consanguineous marriage was brought to dermatology outp...
Neurofibromatosis type1 (NF1) with the incidence of 1 in 3500 births, is the most common disorder wh...
Neurofibromatosis type 1 (NF1) is a rare genetic disorder, characterized by the development of benig...