Literature DB >> 22791546

Diaphragmatic weakness with progressive sensory and motor polyneuropathy: case report of a neonatal IGHMBP2-related neuropathy.

Cyril Gitiaux1, Jean Bergounioux, Maryse Magen, Susana Quijano-Roy, Thierry Blanc, Jean Paul Bonnefont, Isabelle Desguerre.   

Abstract

The authors present a child affected with diaphragmatic paralysis in the early neonatal period. Although no electroneuromyographic abnormalities were reported, the patient developed dramatic motor and respiratory impairment with impossibility to wean from mechanical ventilation. Repeated electroneuromyographic study at age 4 months revealed severe neurogenic changes and sensory nerve abnormalities with more preserved nerve conduction velocities. Genetic studies identified 2 mutations in the gene IGHMBP2. These results support the consideration of this entity as a form of sensory-motor rapidly progressive polyneuropathy rather than a primary anterior horn disease (IGHMBP2-related neuropathy). A review of the series of mutated patients in the French National Database gives new insights of the incidence of this disease in France.

Entities:  

Keywords:  diaphragmatic weakness; infantile neuropathy; palsy; peripheral nervous system diseases; spinal muscular atrophy with respiratory distress type I

Mesh:

Substances:

Year:  2012        PMID: 22791546     DOI: 10.1177/0883073812450209

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  4 in total

1.  Diagnostic exome sequencing identifies two novel IQSEC2 mutations associated with X-linked intellectual disability with seizures: implications for genetic counseling and clinical diagnosis.

Authors:  Stephanie K Gandomi; K D Farwell Gonzalez; M Parra; L Shahmirzadi; J Mancuso; P Pichurin; R Temme; S Dugan; W Zeng; Sha Tang
Journal:  J Genet Couns       Date:  2013-12-04       Impact factor: 2.537

2.  Diagnostic Exome Sequencing and Tailored Bioinformatics of the Parents of a Deceased Child with Cobalamin Deficiency Suggests Digenic Inheritance of the MTR and LMBRD1 Genes.

Authors:  Kelly D Farwell Gonzalez; Xiang Li; Hsiao-Mei Lu; Hong Lu; Joan E Pellegrino; Ryan T Miller; Wenqi Zeng; Elizabeth C Chao
Journal:  JIMD Rep       Date:  2014-03-25

3.  Congenital lethal motor neuron disease with a novel defect in ribosome biogenesis.

Authors:  Russell J Butterfield; Tamara J Stevenson; Lingyan Xing; Tara M Newcomb; Benjamin Nelson; Wenqi Zeng; Xiang Li; Hsiao-Mei Lu; Hong Lu; Kelly D Farwell Gonzalez; Jia-Perng Wei; Elizabeth C Chao; Thomas W Prior; Pamela J Snyder; Joshua L Bonkowsky; Kathryn J Swoboda
Journal:  Neurology       Date:  2014-03-19       Impact factor: 9.910

4.  Diagnostic Odyssey and Application of Targeted Exome Sequencing in the Investigation of Recurrent Infant Deaths in a Syrian Consanguineous Family: a Case of Spinal Muscular Atrophy with Respiratory Distress Type 1.

Authors:  Young A Kim; Hye Young Jin; Yoo-Mi Kim
Journal:  J Korean Med Sci       Date:  2019-02-07       Impact factor: 2.153

  4 in total

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