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[Carlevoix-Saguenay type recessive spastic ataxia. A report of a Spanish case].

作者信息

Pascual-Castroviejo I, Pascual-Pascual S I, Viaño J, Martínez V

机构信息

Servicio de Neurología Pediátrica, Hospital Universitario La Paz, Madrid, España.

出版信息

Rev Neurol. 2000;31(1):36-8.

PMID:10948580
Abstract

OBJECTIVE

To present the first Spanish case, perhaps the first non-Canadian, with ataxia type Charlevoix-Saguenay.

CLINICAL CASE

A patient with important psychomotor delay and non-progressive ataxia has been studied in our Service during the first years of life and his follow-up has been carried out until 30 years of age. He has been studied from the clinical, ophthalmological and neuroradiological with magnetic resonance point of views.

RESULTS

Ataxia and psychomotor delay showed a non-progressive evolution. The patient showed myelinated retinal fibers and atrophy of the superior half of the cerebellum.

CONCLUSION

Neurological, ophthalmological and magnetic resonance images showing atrophy of the superior part of the cerebellum are the three main signs of the ataxia type Charlevoix-Saguenay. This patient could be the first case reported out Canada.

摘要

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引用本文的文献

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Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration.常染色体隐性遗传性痉挛性共济失调(CHARLEVOIX-SAGUENAY 型,ARSACS)的遗传学及 Sacsin 在神经退行性变中的作用。
Int J Mol Sci. 2022 Jan 4;23(1):552. doi: 10.3390/ijms23010552.
2
Autosomal recessive cerebellar ataxias.常染色体隐性遗传性小脑共济失调
Orphanet J Rare Dis. 2006 Nov 17;1:47. doi: 10.1186/1750-1172-1-47.
3
Private SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) families from Turkey.
来自土耳其的夏尔勒沃-萨格奈常染色体隐性痉挛性共济失调(ARSACS)家族中的私有SACS突变。
Neurogenetics. 2004 Sep;5(3):165-70. doi: 10.1007/s10048-004-0179-y. Epub 2004 May 20.