Results 31 to 40 of about 225,381 (184)

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, Salustiano Gomes de Pinho Pessoa, José Everardo Macedo, Débora Juaçaba Cavalcante, Júlio César Garcia de Alencar   +4 more
doaj   +1 more source

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

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

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

Manifestação clínica familiar em pacientes com defeito neuromesoectodérmico Familial clinical manifestation in patients with neuromesoectodermic defect

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, Sandra Lopes Mattos e Dinato, Juliana Messias Moraes, Carla Patrícia Nakanishi, Marcelo Mattos e Dinato   +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, Darren R. Hocking, Hayley Darke, Rachel Mackenzie, Kathryn N. North, Giacomo Vivanti, Jonathan M. Payne   +6 more
wiley   +1 more source

Interventions supporting the empowerment of parent carers of children with neurodisability and other long‐term health conditions: A scoping review

Developmental Medicine &Child Neurology, Volume 68, Issue 4, Page 489-500, April 2026.
This scoping review identified 145 different interventions designed to support parent carer empowerment. These interventions have been catalogued and are presented in an interactive, online database. Abstract Aim To compile information about interventions that have been developed to support the empowerment of parent carers of children and young people ...
Jim Reeder, Morwenna Rogers, Phillip Harniess, Fatema Shamsaddin, Caomhán McGlinchey, Jane R Smith, Sally Kendall, Christopher Morris   +7 more
wiley   +1 more source

Hemifacial spasm in a patient with neurofibromatosis and Arnold-Chiari malformation: a unique case association Espasmo hemifacial em paciente com neurofibromatose e malformação de Arnold-Chiari: uma associação rara

Arquivos de Neuro-Psiquiatria, 2007
BACKGROUND: The association of hemifacial spasm (HFS), Chiari type I malformation (CIM) and neurofibromatosis type 1 (NF1) has not been described yet. CASE REPORT: We report the case of a 31-year-old woman with NF1 who developed a right-sided HFS.
Andre Carvalho Felício, Clecio de Oliveira Godeiro-Junior, Vanderci Borges, Sonia Maria de Azevedo Silva, Henrique Ballalai Ferraz   +4 more
doaj   +1 more source

L'atteinte vésicale au cours de la neurofibromatose de Von Recklinghausen

The Pan African Medical Journal, 2014
La neurofibromatose de type 1 ou maladie de Von Recklinghausen est une maladie génétique autosomique dominante en rapport avec des mutations dans le gène suppresseur de tumeur NF1. L'atteinte uro-génitale au cours de cette maladie est rare et moins de 80
Mohamed Hicham Benazzouz, Tilila Hajjad, Younes Essatara, Hachem El Sayegh, Ali Iken, Lounis Benslimane, Yassine Nouini   +6 more
doaj   +1 more source

Grande tache pigmentée pileuse révélant une forme familiale de la maladie de Von Recklinghausen

The Pan African Medical Journal, 2015
La neurofibromatose de type 1 (NF1) ou maladie de Von Recklinghausen appartient au groupe de maladies appelé phacomatose. C'est une affection autosomique dominante relativement rare.
Anass Es seddiki, Sahar Messaoudi, Dounia Jaafar, Anass Ayyad, Rim Amrani   +4 more
doaj   +1 more source