Results 31 to 40 of about 2,465 (212)

Scleroderma and dentistry: Two case reports [PDF]

, 2016
© 2016 The Author(s).Background: Scleroderma is a chronic connective tissue disorder with unknown etiology. It is characterized by excessive deposition of extracellular matrix in the connective tissues causing vascular disturbances which can result in ...
Bornstein, Michael M., Dixit, Shantanu, Kalkur, Chaithra, Melton, Fred, Sattur, Atul P.   +4 more
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Genetic and clinical characteristics of NEFL-related Charcot-Marie-Tooth disease [PDF]

, 2017
OBJECTIVES: To analyse and describe the clinical and genetic spectrum of Charcot-Marie-Tooth disease (CMT) caused by mutations in the neurofilament light polypeptide gene (NEFL).
Bettencourt, C, Blake, JC, Brandner, S, Gonzalez, MA, Hanna, MG, Horga, A, Houlden, H, Jaunmuktane, Z, Jerath, NU, Laurà, M, Liu, Y-T, Lunn, MP, Manji, H, Poh, R, Polke, JM, Reilly, MM, Shy, M, Wiethoff, S, Züchner, S   +18 more
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Computed Tomographical Characterisation of Dyke-Davidoff-Masson Syndrome: A Case Series [PDF]

Journal of Clinical and Diagnostic Research
Dyke-Davidoff-Masson Syndrome (DDMS) is a rare neurological disorder that primarily manifests through various neurological symptoms, with a significant focus on contralateral hemiparesis and convulsive disorders that often show resistance to standard ...
Krishna Madhukarrao Maske, Kalyani Santosh Jethlia, Anil Gopal Tapdiya, Ameet Chandrakant Panchmahalkar, T Rajalakshmi   +4 more
doaj   +1 more source

Clinical profile of parkinsonism and Parkinson's disease in Lagos, Southwestern Nigeria [PDF]

, 2010
Background Current data on the pattern of parkinsonism and Parkinson's disease in Nigerians are sparse. This database was designed to document the clinical profile of PD in Nigerians, and compare this to prior observations. Methods A database of patients
Njideka U Okubadejo, Oluwadamilola O Ojo, Olajumoke O Oshinaike, NU Okubadejo, BO Osuntokun, BO Osuntokun, BS Schoenberg, BO Osuntokun, N Quinn, JE Ahlskog, A Schrag, MM Hoehn, CG Goetz, Movement Disorder Society Task Force on Rating Scales for Parkinson's Disease, WR Gibb, O Suchowersky, MV Alvarez, JH Bower, M Baldereschi, DF Dluzen, N Pankratz, S Biskup, N Okubadejo, CL Dotchin, NU Okubadejo   +24 more
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Dyke-Davidoff-Masson Syndrome

Journal of Nobel Medical College, 2012
Dyke-Davidoff-Masson Syndrome (DDMS) is characterized by seizures, facial asymmetry, contralateral hemiplegia and mental retardation. The characteristic radiologic features are cerebral hemiatrophy with homolateral hypertrophy of the skull and sinuses ...
Naba Raj Koirala, Roshana Khadka, Manoj Bhattarai, Dibya Tulachan, Ajay Kumar Das, Jwalanta Poudel   +5 more
doaj   +1 more source

Pansclerotic morphea: A male child with hemiatrophy of lower limb

Indian Dermatology Online Journal, 2014
Morphea is a variant of localized scleroderma in which lesions are usually limited to the skin and subcutaneous tissue. Pansclerotic morphea is a rare atrophying and sclerosing type of morphea. It can follow a comparatively benign course with spontaneous
Malay K Dasgupta, Chaitali Patra, Shatanik Sarkar, Sabyasachi Das   +3 more
doaj   +1 more source

Orofacial myofunctional characterization in Parry-Romberg syndrome [PDF]

, 2015
Objetivo: Caracterizar os aspectos miofuncionais orofaciais de pacientes acometidos pela síndrome de Parry-Romberg, por meio de protocolos clínicos padronizados e da Eletromiografia de Superfície (EMGs) dos músculos mastigatórios.
Andrade, Claudia Regina Furquim de, Mangilli, Laura Davison, Rocha, Bruna Rainho, Sassi, Fernanda Chiarion   +3 more
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Hemispherectomy with corpus callosotomy in pediatric Lennox Gastaut Syndrome associated encephalomalacia cyst: The first case in Indonesia [PDF]

, 2022
Lennox-Gastaut syndrome (LGS) is a form of severe epileptic encephalopathy in children. LGS with encephalomalacia cysts is rare in children. We report a six-year-old mentally retarded boy who was referred for an intractable seizure.
Gunawan, P. I., Suryaningtyas, W.
core   +2 more sources

Você conhece esta síndrome? Do you know this syndrome?

Anais Brasileiros de Dermatologia, 2007
Trata-se de criança de oito anos, portadora de atrofia na hemiface direita, desde os seis anos. A ressonância magnética do encéfalo evidenciou espessamento cortical e formação de cistos.
Luciana Baptista Pereira, Rodrigo Santiago Gómez, Cláudia Márcia Resende Silva, Wandilza Fátima dos Santos   +3 more
doaj   +1 more source

Síndrome de moyamoya associada a neurofibromatose tipo I em paciente pediátrico [PDF]

, 2011
CONTEXT: Neurofibromatosis type 1 (NF-1) is the most prevalent autosomal dominant genetic disorder among humans. Moyamoya disease is a cerebral vasculopathy that is only rarely observed in association with NF-1, particularly in the pediatric age range ...
DARRIGO JÚNIOR, Luiz Guilherme, MACHADO, André de Aboim, SANTOS, Antonio Carlos dos, SCRIDELI, Carlos Alberto, TONE, Luiz Gonzaga, VALERA, Elvis Terci   +5 more
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