Abstract
A family is described in which a hereditary peripheral neuropathy occurs, inherited as an autosomal dominant character. The syndrome is present at birth and does not show any significant progression thereafter. Three of the cases have suffered from arthrogryposis multiplex congenita. A secondary myopathy is also present. The condition appears to be intermediary between peroneal muscular atrophy and Friedreich's ataxia. Appearance at birth, presence of arthrogryposis multiplex congenita, and the non-progressive nature separate it sharply from the other heredofamilial ataxias and peripheral neuropathies.
Full text
PDF







Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- HAASE G. R., SHY G. M. Pathological changes in muscle biopsies from patients with peroneal muscular atrophy. Brain. 1960 Dec;83:631–637. doi: 10.1093/brain/83.4.631. [DOI] [PubMed] [Google Scholar]
- Kaeser H. E. Scapuloperoneal muscular atrophy. Brain. 1965 Jun;88(2):407–418. doi: 10.1093/brain/88.2.407. [DOI] [PubMed] [Google Scholar]
- SMITH E. M., BENDER L. F., STOVER C. N. Lower motor neuron deficit in arthrogryposis. An EMG study. Arch Neurol. 1963 Jan;8:97–100. doi: 10.1001/archneur.1963.00460010113013. [DOI] [PubMed] [Google Scholar]







