Document Detail


Spinal muscular atrophy with progressive myoclonic epilepsy: report of new cases and review of the literature.
MedLine Citation:
PMID:  12571787     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Spinal muscular atrophy (SMA) is a clinically and genetically heterogeneous disease characterised by loss of motor function and muscle atrophy due to anterior horn cell degeneration. The most common variant is chromosome 5-linked proximal SMA, ranging in severity from congenital onset and infantile death to onset in adult life. Genetically separate variants with different distribution of weakness and/or additional features such as central nervous system involvement have been described. A rare variant with associated myoclonic epilepsy and lower motor neuron disease had been previously described in three families before the SMN gene, responsible for the common form of SMA, was isolated. We report four patients from two additional families affected by a syndrome characterised by severe and progressive myoclonic epilepsy and proximal weakness, tremor and lower motor neuron disease proven by electrophysiologic and muscle biopsy findings. Extensive metabolic investigations were normal and genetic analysis excluded the SMN gene. This study confirms that the association of myoclonic epilepsy and motor neuron disease represents a separate clinical and genetic entity from chromosome 5-linked SMA, the primary defect of which remains unknown.
Authors:
G Haliloglu; A Chattopadhyay; L Skorodis; A Manzur; E Mercuri; B Talim; Z Akçören; Y Renda; F Muntoni; H Topaloğlu
Related Documents :
2896627 - Long-range genomic map of the duchenne muscular dystrophy (dmd) gene: isolation and use...
12438487 - Clinical and genetic heterogeneity in peroneal muscular atrophy associated with vocal c...
7795607 - Linkage of posterior polymorphous corneal dystrophy to 20q11.
16861757 - Combined fluorescence in situ hybridization and prins for the analysis of the dystrophi...
18680737 - Cryotops versus open-pulled straws (ops) as carriers for the cryopreservation of bovine...
23853517 - Construction of a chromosome-assigned, sequence-tagged linkage map for the radish, raph...
Publication Detail:
Type:  Case Reports; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Neuropediatrics     Volume:  33     ISSN:  0174-304X     ISO Abbreviation:  Neuropediatrics     Publication Date:  2002 Dec 
Date Detail:
Created Date:  2003-02-06     Completed Date:  2003-04-23     Revised Date:  2008-01-16    
Medline Journal Info:
Nlm Unique ID:  8101187     Medline TA:  Neuropediatrics     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  314-9     Citation Subset:  IM    
Affiliation:
Department of Child Neurology, Hacettepe Children's Hospital, Ankara, Turkey.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Biopsy
Cerebral Cortex / physiopathology
Child
Child, Preschool
Chromosome Aberrations
Chromosomes, Human, Pair 5
Consanguinity
Electroencephalography
Epilepsies, Myoclonic / diagnosis*,  genetics,  physiopathology
Female
Follow-Up Studies
Genes, Recessive
Humans
Infant
Infant, Newborn
Male
Muscle, Skeletal / pathology
Neurologic Examination
Phenotype
Spinal Muscular Atrophies of Childhood / diagnosis*,  genetics,  physiopathology

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Microlissencephaly in microcephalic osteodysplastic primordial dwarfism: a case report and review of...
Next Document:  Refractory photosensitive epilepsy associated with a complex rearrangement of chromosome 2.