Literature DB >> 572450

[Arthogryposis multiplex congenita with neurogenic atrophy and brachydactyly (author's transl)].

U Eckel, J Spranger, H Klein.   

Abstract

Case report of arthrogryposis multiplex congenita with histologically proved neutrogene atrophy of muscles. The also existing reduction deformities of the limbs, showing aplasia and hypoplasia of phalanges may hypothetically be of neuropathic origin.

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Year:  1979        PMID: 572450

Source DB:  PubMed          Journal:  Klin Padiatr        ISSN: 0300-8630            Impact factor:   1.349


  1 in total

1.  A dominantly inherited lower motor neuron disorder presenting at birth with associated arthrogryposis.

Authors:  P Fleury; G Hageman
Journal:  J Neurol Neurosurg Psychiatry       Date:  1985-10       Impact factor: 10.154

  1 in total

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