نتایج جستجو برای: Arthrogryposis

تعداد نتایج: 1172  

Journal: :AJNR. American journal of neuroradiology 2017
M F V V Aragao A M Brainer-Lima A C Holanda V van der Linden L Vasco Aragão M L M Silva Júnior C Sarteschi N C L Petribu M M Valença

BACKGROUND AND PURPOSE Arthrogryposis is among the malformations of congenital Zika syndrome. Similar to the brain, there might exist a spectrum of spinal cord abnormalities. The purpose of this study was to explore and describe in detail the MR imaging features found in the spinal cords, nerve roots, and brains of children with congenital Zika syndrome with and without arthrogryposis. MATERI...

2018
Allen L. Ho Jyodi Mohole Eric S. Sussman Arjun V. Pendharkar Harminder Singh

Arthrogryposis multiplex congenita is a rare, nonprogressive congenital disorder that describes a constellation of conditions characterized by multiple joint contractures. Spinal pathology and deformity are common; however, the majority of the literature on arthrogryposis is focused on pediatric management. There exist very few reports on long-term outcomes and management of adults with arthrog...

2015
Perrine Venot Philippe Vo Van Gratiella Mac Caby Gauthier Loron Jean Paul Bory Ahmad Akhavi Nathalie Bednarek

Arthrogryposis multiplex congenita is a syndromic condition defined by contracture of 2 or more joints. A large range of etiologies has been reported such as neuromuscular disorders (peripheral dysfunction), chromosomal abnormalities, or cerebral malformations (central dysfunction) leading to fetal immobility. Severity of arthrogryposis depends on the etiology and duration of fetal immobility. ...

Journal: :Journal of medical genetics 1993
C T Schrander-Stumpel C J Höweler A D Reekers N M De Smet J G Hall J P Fryns

Arthrogryposis multiplex congenita is a heterogeneous condition and many different types are clinically recognisable. Recently, a new type of autosomal dominant arthrogryposis was described in a father and son. We report on a male patient with similar clinical features, confirming this distinct type of arthrogryposis. The condition is characterised by congenital contractures of the hands and fe...

Journal: :The Journal of bone and joint surgery. American volume 2011
David M Alvarado Jillian G Buchan Christina A Gurnett Matthew B Dobbs

BACKGROUND Few genes responsible for distal arthrogryposis type 1 are known, although genes coding for the proteins in the sarcomere have been implicated in other types of distal arthrogryposis. Cost-effective sequencing methods are now available to examine all genes in the human genome for the purpose of establishing the genetic basis of musculoskeletal disorders. METHODS A multigenerational...

Journal: :The Journal of bone and joint surgery. American volume 2009
Michael Bamshad Ann E Van Heest David Pleasure

C ongenital contractures can be divided into two groups: isolated contractures and multiple contractures (Fig. 1). Isolated congenital contractures affect only a single area of the body; the most common isolated contracture is congenital clubfoot, which occurs in one of every 500 live births. The term arthrogryposis is often used as shorthand to describe multiple congenital contractures that af...

2017
R. Kalirajan

Arthrogryposis, is one of the congenita anomalies reported in cattle and other domestic animals, is an extreme form of contracted tendons in which many joints are in flexed state. The present report about a rare case of dystocia due to Arthrogryposis multiplex foetus in a HF cross cow which was relieved per vaginally by traction. Keyword: Dystocia, traction, pervaginal, Arthrogryposis, HF cross...

2017
Manouchehr Safdarian Mahdi Safdarian

Management of spinal deformities in a patient with arthrogryposis can be challenging for spine surgeons. The literature about the accompaniment of scoliosis; the most common spine deformity reported in arthrogryposis, is still poor. Moreover, the development of cervical kyphosis and thoracic lordoscoliosis in a patient with arthrogryposis is much rare. This paper reports a 26-year-old medical d...

Journal: :Brain & development 2010
Annapurna Poduri Vida Chitsazzadeh Stefano D'Arrigo Ermellina Fedrizzi Chiara Pantaleoni Daria Riva Claudia Busse Helmut Küster Adre Duplessis John Gaitanis Mustafa Sahin Cheryl Garganta Meral Topcu Kira A Dies Brenda J Barry Jennifer Partlow A James Barkovich Christopher A Walsh Bernard S Chang

BACKGROUND Bilateral perisylvian polymicrogyria (BPP) is a well-recognized malformation of cortical development commonly associated with epilepsy, cognitive impairment, and oromotor apraxia. Reports have suggested the association of BPP with arthrogryposis multiplex congenita. We sought to investigate the clinical, electrophysiological, and neuroradiological features of this combined syndrome t...

Journal: :American journal of medical genetics. Part A 2013
Judith G Hall

In a review of 2,300 cases of arthrogryposis collected over the last 35 years, 33 cases of maternal uterine structural anomalies were identified (1.3%). These cases of arthrogryposis represent a very heterogeneous group of types of arthrogryposis. Over half of individuals affected with arthrogryposis demonstrated asymmetry and some responded to removal of constraint, 29 of the 33 cases of arthr...

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