Results 31 to 40 of about 1,927 (190)

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
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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, Hugo José de Araújo, Aloysio Campos da Paz Júnior   +2 more
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, Salustiano Gomes de Pinho Pessoa, José Everardo Macedo, Débora Juaçaba Cavalcante, Júlio César Garcia de Alencar   +4 more
doaj   +1 more source

Hyperthyroidism related to McCune-Albright syndrome: report of two cases and review of the literature [PDF]

, 2008
INTRODUCTION: McCune-Albright syndrome is a sporadic disease clinicaly characterized by polyostotic fibrous dysplasia, café-au-lait cutaneous spots and hyperfunctional endocrinopathies, such as precocious puberty, hyperthyroidism, acromegaly and others ...
Abs R, Albin J, Albright F, Ana Carolina R. Sallum, Andrews SB, Benedict P, Brogan P, Cavanah SFW, Cohen MM Jr, de Sanctis C, Domenech E, D’Armiento M, Fernando D. Leonhardt, Feuillan PP, Feuillan PP, Firat D, Gallacher SJ, Giovanelli G, Halvorsen S, Hamilton CR Jr, Huang TS, Isotani H, Jervis GA, Kim JP, Lair-Milan F, Lawless ST, Lee PA, Leet AI, Mastorakos G, Mastorakos G, Mauras N, McCune DJ, Misaki M, Moldawer M, Márcio Abrahão, Onivaldo Cervantes, Peck FB, Reinaldo K. Yazaki, Richton SM, Riminucci M, Samuel S, Schwindinger WF, Shenker A, Shenker A, Sternberg WH, Summerfeldt P, Tanaka T, Vague J, Weinstein LS, Yettra M, Yoshimoto M, Zangeneh F   +51 more
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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

Syndrome in question [PDF]

, 2016
Neurofibromatosis is extremely variable in its presentation. Segmental neurofibromatosis (SNF), which corresponds to NF-type 5 in the Riccardi classification, is a rare disorder. It may go unrecognized if few lesions are observed.
Carvalho, S., Horta, M., Oujo, E., Rosmaninho, A.   +3 more
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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

Phaeochromocytoma Associated to Von Recklinghausen Neurofibromatosis Type I: a Rare Clinical Case [PDF]

, 2011
Os feocromocitomas são neoplasias originárias das células cromafins da crista neural localizados, na sua grande maioria, na medula supra-renal, podendo também aparecer nos gânglios simpáticos (paragangliomas).
Jorge, V, Noronha, C, Pires da Silva, I, Riscado, M, Sousa, M   +4 more
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