Juvenile amyotrophic lateral sclerosis

被引：6

作者：

Anju Aggarwal

机构：

[1] Guru Tegh Bahadur Hospital,Department of Pediatrics, University College of Medical Sciences

来源：

The Indian Journal of Pediatrics | 2006年 / 73卷 / 3期

关键词：

Juvenile amyotrophic lateral sclerosis; Early onset;

D O I：

10.1007/BF02825486

中图分类号：

学科分类号：

摘要：

Juvenile amytrophic lateral sclerosis (JALS) is a type of motor neuron disease presenting before 25 years of age. It is characterized by a combination of upper and lower motor signs. It may be familial or sporadic. We are reporting a sporadic case of JALS with onset of symptoms at 4 years of age. Diagnostic criteria and a brief review of literature are presented.

引用

页码：225 / 226

页数：1

共 36 条

[1]

Ben Hamida M(1990)Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis) Brain 13 347-363

[2]

Hentati F(1982)A new hypothesis of etiology of amytrophic lateral sclerosis: the DNA hypothesis Arch Neurol 39 677-680

[3]

Ben Hamida C(1954)Amyotrophic familial spastic paraplegia Neurology 4 40-47

[4]

Bradley WG(1999)Autosomal dominant juvenile amyotrophic lateral sclerosis Brain 122 1539-1550

[5]

Krasin F(1981)Wasted leg syndrome. A clinical, electrophysiological and histological study Clinical Neuro Neurosurg 83 19-19

[6]

Refums Skillicon SA(2003)Juvenile amyotrophic lateral sclerosis with unusual presentation: A case report Neurol India 51 413-414

[7]

Rabin BA(1993)Mutations in the Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis Nature 362 59-62

[8]

Griffin JW(1994)Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35 Nat Genet 7 425-428

[9]

Crain BJ(2002)Autosomal dominant juvenile amytrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for same disorder? Brain 125 1320-1325

[10]

Prabhakar S(1980)Plasmapheresis in amytrophic lateral sclerosis Ann Neurol 8 644-645

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