Codi QR

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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Md. Fekarul Islam, Devdeep Mukherjee, Ritabrata Kundu, Joydeep Das
Format: Artigo
Idioma:Inglês
Publicat: Krishna Vishwa Vidyapeeth (Deemed to be University), Karad 2015-01-01
Col·lecció:Journal of Krishna Institute of Medical Sciences University
Matèries:
Accés en línia:http://jkimsu.com/jkimsu-vol4no1/JKIMSU,%20Vol.%204,%20No.%201,%20Jan-Mar%202015%20Page%20139-141.pdf
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!