Literature DB >> 3978931

Neuropathologic aspects of arthrogryposis multiplex congenita.

B Q Banker.   

Abstract

Arthrogryposis multiplex congenita is not a specific disorder but rather a symptom complex of congenital joint contractures associated with both neurogenic and myopathic disorders. Pathologic studies, including autopsy evaluation and muscle biopsy alone, were performed on 74 children with features of arthrogryposis. In 69 children (93%), the deformities were found to be neurogenic in origin, while five (7%) had myopathic disorders. The children in these two groups could be subdivided into 17 specific disorders, depending on the site of the pathologic lesions: anterior horn cells, roots, peripheral nerves, motor end-plates, or muscle. Disorders associated with dysgenesis of anterior horn cells were the most common pathologic type. The neurogenic groups were also characterized by a high incidence of other congenital anomalies, while the myopathic group had few associated defects. The main feature shared by these disorders appears to be the presence of severe weakness early in fetal development, which immobilizes joints, resulting in contractures.

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Year:  1985        PMID: 3978931

Source DB:  PubMed          Journal:  Clin Orthop Relat Res        ISSN: 0009-921X            Impact factor:   4.176


  4 in total

1.  Plasma from human mothers of fetuses with severe arthrogryposis multiplex congenita causes deformities in mice.

Authors:  L Jacobson; A Polizzi; G Morriss-Kay; A Vincent
Journal:  J Clin Invest       Date:  1999-04       Impact factor: 14.808

2.  A case of congenital bilateral absence of elbow flexor muscles: review of differential diagnosis and treatment.

Authors:  David T Netscher; Oluseyi Aliu; Saleh Samra; Eric Lewis
Journal:  Hand (N Y)       Date:  2007-10-09

3.  Arthrogryposis: an update on clinical aspects, etiology, and treatment strategies.

Authors:  Bartłomiej Kowalczyk; Jarosław Feluś
Journal:  Arch Med Sci       Date:  2016-02-02       Impact factor: 3.318

4.  Arthrogryposis multiplex congenital in a child manifesting phenotypic features resembling dysosteosclerosis/osteosclerosis malformation complex; 3DCT scan analysis of the skull base.

Authors:  Ali Al Kaissi; Georg Kalchhauser; Franz Grill; Klaus Klaushofer
Journal:  Cases J       Date:  2008-07-23
  4 in total

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