论文部分内容阅读
OBJECTIVE:To describe the clinical features of a novel variant of autosomal recessive lower motor neuron disease(LMND)with childhood onset and to map the disease-causing gene.METHODS:The authors performed a clinical study in a large consanguineous African family.After linkage exclusion to SMN1 and SOD1 loci,they performed a genome-wide linkage analysis to map the underlying genetic defect.RESULTS:This novel variant of LMND with childhood onset and autosomal recessive mode of inheritance is characterized by a progressive symmetric and generalized involvement of the musculature.Four of the five affected patients had muscle weakness since age 3,strongly worsening during childhood and leading to generalized tetraplegia in adulthood.Genetic analyses using homozygosity mapping strategy assigned this progressive generalized LMND locus to an interval of 3.9 cM(or 1.5 megabases)on chromosome 1p36,between loci D1S508 and D1S2633(Zmax =3.79 at θ= 0.00 at locus D1S253).This region encloses 27 candidate genes.CONCLUSION:Genetic mapping of a novel rare phenotype of lower motor neuron disease opens the way toward the identification of a new gene involved in motor neuron degeneration,located in the 1p36 chromosomal region.
OBJECTIVE: To describe the clinical features of a novel variant of autosomal recessive lower motor neuron disease (LMND) with childhood onset and map to the disease-causing gene. METHODS: The authors performed a clinical study in a large consanguineous African family. After linkage exclusion to SMN1 and SOD1 loci, they performed a genome-wide linkage analysis to map the underlying genetic defect. RESULTS: This novel variant of LMND with childhood onset and autosomal recessive mode of inheritance is characterized by a progressive symmetric and generalized involvement of the musculature . Focus of the five affected patients had muscle weakness since age 3, strongly worsening during childhood and leading to generalized tetraplegia in adulthood. Genetic analyzes using homozygosity mapping strategy assigned this progressive generalized LMND locus to an interval of 3.9 cM (or 1.5 megabases) on chromosome 1p36, between loci D1S508 and D1S2633 (Zmax = 3.79 at θ = 0.00 at locus D1S253). This region encloses 27 can didate genes.CONCLUSION: Genetic mapping of a novel rare phenotype of lower motor neuron disease opens the way toward the identification of a new gene involved in motor neuron degeneration, located in the 1p36 chromosomal region.