| Literature DB >> 18263757 |
Angela M Kaindl1, Ulf-Peter Guenther, Sabine Rudnik-Schöneborn, Raymonda Varon, Klaus Zerres, Markus Schuelke, Christoph Hübner, Katja von Au.
Abstract
Autosomal recessive spinal muscular atrophy with respiratory distress type 1 (SMARD1), recently referred to as distal spinal muscular atrophy 1 (DSMA1; MIM#604320) and also known as distal hereditary motor neuropathy type 6 (dHMN6 or HMN6), results from mutations in the IGHMBP2 gene on chromosome 11q13.3 encoding the immunoglobulin micro-binding protein 2. In contrast to the infantile spinal muscular atrophy type 1 (SMA1; Werdnig-Hoffmann disease) with weakness predominantly of proximal muscles and bell-shaped thorax deformities due to intercostal muscle atrophy, infants with distal spinal muscular atrophy 1 usually present with distal muscle weakness, foot deformities, and sudden respiratory failure due to diaphragmatic paralysis that often requires urgent intubation. In this article, the authors review the clinical, neuropathological, and genetic aspects of distal spinal muscular atrophy 1 and discuss differential diagnoses.Entities:
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Year: 2008 PMID: 18263757 DOI: 10.1177/0883073807310989
Source DB: PubMed Journal: J Child Neurol ISSN: 0883-0738 Impact factor: 1.987