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Friedreich's Ataxia – A Clinical Diagnosis

Friedreich's ataxia (FA) is an autosomal recessive spinocerebellar degenerative disease characterized by hyperexpansion of GAA triplets in Frataxin gene. The hallmark of this disorder is ataxic gait, areflexia, Babinski's sign and positive Romberg test. We report a 9 year old child who presente...

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Bibliografski detalji
Glavni autori: Md. Fekarul Islam, Devdeep Mukherjee, Ritabrata Kundu, Joydeep Das
Format: Artigo
Jezik:Inglês
Izdano: Krishna Vishwa Vidyapeeth (Deemed to be University), Karad 2015-01-01
Serija:Journal of Krishna Institute of Medical Sciences University
Teme:
Online pristup:http://jkimsu.com/jkimsu-vol4no1/JKIMSU,%20Vol.%204,%20No.%201,%20Jan-Mar%202015%20Page%20139-141.pdf
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