Results 31 to 40 of about 1,890 (196)
Plexiform neurofibroma of the upper limb Neurofibroma plexiforme de membro superior
Revista Brasileira de Cirurgia Plástica, 2011 The authors present an unusual case of plexiform neurofibroma affecting the upper limb in a patient diagnosed with type 1 neurofibromatosis. Tumor resection was performed on the median nerve.
Kátia Torres Batista +2 more
doaj +1 more source
Desvios Axiais dos Membros Inferiores [PDF]
, 2009 As deformidades axiais dos membros inferiores constituem um dos principais motivos de consulta na área de Ortopedia Infantil. Esta situação deve-se, por um lado, ao facto de haver uma grande percentagem de crianças (cerca de 20%) que apresentam uma ...
Campagnolo, J, Cassiano Neves, M
core +2 more sources
Maladie de Von Recklinghausen compliquée de Neurofibromes plexiformes cervico-faciaux
The Pan African Medical Journal, 2015 La neurofibromatose de type 1 (NF1), appelée également maladie de Von Recklinghausen, est une affection autosomique dominante caractérisée par son polymorphisme clinique.
Madiha Mahfoudhi, Khamassi Khaled
doaj +1 more source
Abordagem cirúrgica de neurofibroma gigante Surgical correction of a giant neurofibroma
Revista Brasileira de Cirurgia Plástica, 2012 Neurofibromatose é uma doença de origem genética autossômica dominante composta por três tipos: neurofibromatose tipo 1 (NF1), neurofibromatose tipo 2 (NF2) e schwannomatose.
Iana Silva Dias +4 more
doaj +1 more source
Tumor Maligno da Bainha de Nervo Periférico em Doente com Neurofibromatose Tipo 1: Caso Clínico [PDF]
, 2019 Neurofibromatosis type 1 is an autosomal dominant disease, with neurofibroma being the hallmark of this disease. Malignant peripheral nerve tumors are more frequent in neurofibromatosis type 1 and may result from the transformation of neurofibromas ...
Duarte, Artur +3 more
core +2 more sources
Neurofibromatose type 1 : à propos d´un cas
PAMJ Clinical Medicine, 2020 Nous rapportons le cas d´un patient de 30 ans , qui a comme antécédent une consanguinité de 1er degré, qui consulte pour une baisse de l´acuité visuelle progressive aux deux yeux.
Alae El Bouaychi, Fatiha Boudguigue
doaj +1 more source
Múltiplos defeitos localizados da camada de fibras nervosas em um paciente com glioma de nervo óptico no olho contralateral: relato de caso [PDF]
, 2009 This case report describes a young non-glaucomatous patient with neurofibromatosis and previous history of optic nerve glioma, which developed multiple wedge-shaped retinal nerve fiber layer defects close to a chorioretinal scar in the fellow eye.
Lima, Verônica Castro +4 more
core +3 more sources
Nodules de lisch dans la maladie de Von Recklinghausen
PAMJ Clinical Medicine, 2019 La maladie de Von Recklinghausen est une maladie systémique génétique et hétérogène. L´atteinte oculaire au cous de cette phacomatose est rare mais pathognomonique.
Kawtar Hessaki
doaj +1 more source
Arquivos de Neuro-Psiquiatria, 2006 Relatamos a associação de dois casos distintos de neuromesoectodermose ocorridos em uma mesma família, um manifestado através da neurofibromatose tipo 1 e outro através da esclerose tuberosa.
Maria Lúcia Leal dos Santos +4 more
doaj +1 more source
Socially oriented attention in young children with neurofibromatosis type 1: An eye‐tracking study
Developmental Medicine &Child Neurology, Volume 68, Issue 4, Page 541-548, April 2026.Plain language summary: https://onlinelibrary.wiley.com/doi/10.1111/dmcn.70050 Abstract Aim To examine visual engagement to social stimuli and response to joint attention in young children with neurofibromatosis type 1 (NF1) and typically developing peers (controls). Method Forty‐five preschool children were studied cross‐sectionally (mean age [SD] = 4
Kristina M. Haebich +6 more
wiley +1 more source