نتایج جستجو برای: arthrogryposis

تعداد نتایج: 1172  

Journal: :Journal of medical genetics 1981
V B Penchaszadeh B Salszberg

The multiple pterygium syndrome is a rare autosomal recessive condition characterised by arthrogryposis multiplex congenita, pterygia of the neck, fingers, and antecubital, popliteal, and intercrural areas, growth retardation, and facial, vertebral, and genital anomalies. We present two unrelated patients of 17 and 6 years of age, respectively, affected with this condition. We describe the natu...

2013

Veterinary Ireland Journal Volume 3 Number 5 259 SOUTH-EAST REGION BoVINE ABoRtIoN AND CoNgENItAl DISEASE Schmallenberg Virus Kilkenny RVL suspected Schmallenberg Virus as the cause of a bizarre deformity of the head of a full term bovine foetus. Both upper and lower jaws were short and upturned and there was a single central eye (Fig 1). There was also arthrogryposis and hydranencephaly. PCR w...

2015
Eva Pontén

Arthrogryposis is defined as limited range of motion in three or more joints in two or more body parts. This article will describe treatment options for the arthrogrypotic knee. In all types of arthrogryposis, and in both extension and flexion deformities, very early treatment is favorable. Just after birth, traction and mobilization followed by serial casting could often greatly improve the ra...

2015
Hamza Sucuoglu Nurettin Irem Ornek Cagkan Caglar

Arthrogryposis multiplex congenita (AMC) is a syndrome characterized by nonprogressive multiple congenital joint contractures. The etiology of disease is multifactorial; it is most commonly suspected from absent fetal movements and genetic defects. AMC affects mainly limbs; also it might present with other organs involvement. It is crucial that the diagnosis of AMC should be kept in mind by mus...

2012
Emmanouil Kalampokas Theodoros Kalampokas Chrisostomos Sofoudis Efthymios Deligeoroglou Dimitrios Botsis

Arthrogryposis multiplex congenita (AMC) refers either to a syndromic or to a nonsyndromic group of conditions with varied etiology and complex clinical features, including multiple congenital contractures in different body areas. Its etiology still remains unclear but generally any cause that leads to reduced fetal movement may lead to congenital contractures and in severe cases to fetal akine...

2013
Asim Kumar Kundu

Freeman-Sheldon Syndrome (FSS), or distal arthrogryposis type 2A, is a rare congenital myopathy and dysplasia characterized by multiple contractures, abnormalities of the head and face, defective development of the hands and feet and skeletal malformations. The facial muscle contracture produces the typical “whistling face” appearance. Anesthetic issues include difficult intravenous access, dif...

2017
Burcu BAL Nurhan GULER

Mandibular hypomobility results from various disorders affecting the stomatognathic system. Arthrogryposis multiplex congenita (AMC) is an uncommon systemic disorder with mandibular hypomobility involved. Notably few cases of AMC with limited mouth opening and reduced range of jaw movement have been described in which this restriction has been attributed to involvement of the coronoid process. ...

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