نتایج جستجو برای: arthrogryposis

تعداد نتایج: 1172  

Journal: :The Journal of bone and joint surgery. British volume 1984
A D Green J A Fixsen G C Lloyd-Roberts

Eighteen patients (34 feet) with arthrogryposis multiplex congenita treated by talectomy for rigid equinovarus deformity were reviewed. The average follow-up was 11 years. Twenty-four feet (71%) were considered satisfactory; the remainder were improved. Seven feet required further operations to correct recurrence of the deformity, but finally all could be fitted with boots or shoes and all pati...

2017
Yoshimasa Hirashima Shoei Kitahara Tomoko Kato Hiroaki Shirafuji Shogo Tanaka Tohru Yanase

In 2015 and 2016, we observed 15 malformed calves that were exposed to intrauterine infection with Shamonda virus, a Simbu serogroup orthobunyavirus, in Japan. Characteristic manifestations were arthrogryposis and gross lesions in the central nervous system. Our results indicate that this arbovirus should be considered a teratogenic virus in ruminants.

Journal: :Journal of neurology, neurosurgery, and psychiatry 1985
P Fleury G Hageman

Of a family consisting of 54 members, 44 were examined. Twenty-one showed signs of a clinically non-progressive congenital lower motor neuron disorder restricted to the lower part of the body, which resulted in arthrogryposis in 15 cases. The mode of inheritance is autosomal dominant with very varied expression of the gene.

Journal: :Annals of child neurology 2022

PurposeWieacker-Wolff syndrome is a rare disease caused by X-linked zinc finger C4H2-type containing (ZC4H2) mutations. It characterized arthrogryposis multiplex congenita (AMC) and intellectual disability (ID), including impairment of central peripheral synaptic plasticity. Currently, it named “ZC4H2-associated disease” (ZARD) due to various clinical features other than AMC ID. Here, we report...

Journal: :Orphanet journal of rare diseases 2015
Emily J Todd Kyle S Yau Royston Ong Jennie Slee George McGillivray Christopher P Barnett Goknur Haliloglu Beril Talim Zuhal Akcoren Ariana Kariminejad Anita Cairns Nigel F Clarke Mary-Louise Freckmann Norma B Romero Denise Williams Caroline A Sewry Alison Colley Monique M Ryan Cathy Kiraly-Borri Padma Sivadorai Richard J N Allcock David Beeson Susan Maxwell Mark R Davis Nigel G Laing Gianina Ravenscroft

BACKGROUND Fetal akinesia/hypokinesia, arthrogryposis and severe congenital myopathies are heterogeneous conditions usually presenting before or at birth. Although numerous causative genes have been identified for each of these disease groups, in many cases a specific genetic diagnosis remains elusive. Due to the emergence of next generation sequencing, virtually the entire coding region of an ...

2017
Mohamed Taieb Mohamed Taieb Kassab

Arthrogryposis is an orthopedic condition characterized by greater or lesser stiffness at the four members and less frequently of the spine. Treatment is with certain orthopedic surgical indications in functional aim. The purpose of this work is to present a complex case of arthrogryposis multiplex congenita with partially reversible neurological complications following spinal surgery. Presenta...

2010
D E Emmanouil

This report describes a case of Arthrogryposis Multiplex Congenita (AMC) with limited mouth opening and dental caries. Conservative dental treatment and physiotherapy exercises were prescribed. The aim of this case report is to describe the method and difficulties in the dental care of this patient and outline the importance of a preventive programme.

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