نتایج جستجو برای: arthrogryposis

تعداد نتایج: 1172  

Journal: :Hand clinics 2009
Jennifer M Ty Michelle A James

The term "failure of differentiation" describes the phenotypes of a large number of otherwise unrelated conditions. The six conditions described here (arthrogryposis, camptodactyly, clinodactyly, Madelung deformity, trigger finger, and trigger thumb) are believed to occur because various structures failed to differentiate normally; however, they have neither common features nor a common cause. ...

Journal: :The Journal of bone and joint surgery. British volume 1980
L M Brown M J Robson W J Sharrard

Eleven patients with arthrogryposis multiplex congenita neurologica have been reviewed. Distinct patterns of deformity and muscle activity were identified which have been correlated with specific levels of segmental neurological motor deficit without sensory loss. The clinical picture was consistent with localised lesions of the anterior horn cell cell columns. This finding agreed with the reco...

Journal: :Revista brasileira de ortopedia 2010
Luis Eduardo Munhoz da Rocha Fábio Koiti Nishimori Daniel Carvalho de Figueiredo Dulce Helena Grimm Luiz Antonio Munhoz da Cunha

UNLABELLED To evaluate the results from surgical treatment of hip dislocation through the anteromedial approach, in patients with arthrogryposis multiplex congenita (AMC). METHODS The medical files and radiographs of seven children with AMC who presented hip dislocation (total of 10 dislocated hips) were retrospectively reviewed. Pre and postoperative joint mobility was evaluated by summing t...

Journal: :Neurology 2015
Mariacristina Scoto Alexander M Rossor Matthew B Harms Sebahattin Cirak Mattia Calissano Stephanie Robb Adnan Y Manzur Amaia Martínez Arroyo Aida Rodriguez Sanz Sahar Mansour Penny Fallon Irene Hadjikoumi Andrea Klein Michele Yang Marianne De Visser W C G Truus Overweg-Plandsoen Frank Baas J Paul Taylor Michael Benatar Anne M Connolly Muhammad T Al-Lozi John Nixon Christian G E L de Goede A Reghan Foley Catherine Mcwilliam Matthew Pitt Caroline Sewry Rahul Phadke Majid Hafezparast W K Kling Chong Eugenio Mercuri Robert H Baloh Mary M Reilly Francesco Muntoni

OBJECTIVE To expand the clinical phenotype of autosomal dominant congenital spinal muscular atrophy with lower extremity predominance (SMA-LED) due to mutations in the dynein, cytoplasmic 1, heavy chain 1 (DYNC1H1) gene. METHODS Patients with a phenotype suggestive of a motor, non-length-dependent neuronopathy predominantly affecting the lower limbs were identified at participating neuromuscu...

2008
Andrea Rossi Hania Zlotnik

Rossi’s paper is well organized and generally clear. The most complete and useful part is that relating to children left behind (chapter 2). The impact of migration on those children has been the focus of considerable attention by the research community. Rossi does a good job of detailing the main findings of the research literature. His review shows that there are few findings that could be tr...

2014
Jiang-Li Tan Kees Van Achterberg Xue-Xin Chen

Twenty two species of the paper wasp genus Ropalidia Guérin-Méneville, 1831, are listed from China. Among them, R. malaisei van der Vecht, 1962, R. cyathiformis (Fabricius, 1804), R. santoshae Das & Gupta, 1989, R. scitula (Bingham, 1897), R. obscura Gusenleitner, 1996 and R. ornaticeps (Cameron, 1900) are new records from China. A new species, R. parartifex Tan & van Achterberg, is described. ...

Journal: :Arquivos De Neuro-psiquiatria 2023

Case presentation: Male patient, 1 year-old, born and resident in Maranhão. Mother reported reduced fetal movement, after birth some dysmorphisms were identified such as deformity the lower limbs, characterized by arthrogryposis, bilateral congenital clubfoot, dislocation of hip fracture right femur perceived on fifth day life. During development, generalized hypotonia significant motor delay n...

2016
Gabriele Tonni Gianpaolo Grisolia Eduardo Félix Santana Edward Araujo Júnior

AIM To show imaging results from application of four-dimensional (4D) ultrasound lightening technique (HDlive™) in clinical obstetrics practice. METHODS Normal and abnormal fetuses at second and third trimester of pregnancy undergoing routine scan with 4D HDlive™ (5DUS) in the rendering mode are described. Realistic features of fetal structures were provided by 5DUS in the rendering mode. Nor...

Journal: :Orphanet Journal of Rare Diseases 2009
Reha M Toydemir Michael J Bamshad

Sheldon-Hall syndrome (SHS) is a rare multiple congenital contracture syndrome characterized by contractures of the distal joints of the limbs, triangular face, downslanting palpebral fissures, small mouth, and high arched palate. Epidemiological data for the prevalence of SHS are not available, but less than 100 cases have been reported in the literature. Other common clinical features of SHS ...

Journal: :The Journal of bone and joint surgery. British volume 1998
H Akazawa K Oda S Mitani T Yoshitaka K Asaumi H Inoue

Arthrogryposis multiplex congenita (AMC) is a rare disease with multiple joint contractures. It is widely believed that bilaterally dislocated hips should not be reduced since movement is satisfactory and open reduction has had poor results. Since 1977 we have performed a new method of open reduction using an extensive anterolateral approach on ten hips in five children with AMC. The mean age a...

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