Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/34443
Title: Severe brain involvement in 5q spinal muscular atrophy type 0
Authors: MENDONCA, Rodrigo H.ROCHA, Antonio J.LOZANO-ARANGO, AndresDIAZ, Astry B.CASTIGLIONI, ClaudiaSILVA, Andre M. S.REED, Umbertina C.KULIKOWSKI, LesliePARAMONOV, IdaCUSCO, IvonTIZZANO, Eduardo F.ZANOTELI, Edmar
Citation: ANNALS OF NEUROLOGY, v.86, n.3, p.458-462, 2019
Abstract: Spinal muscular atrophy (SMA) type 0 is the most severe form of SMA, associated with the SMN1 gene and manifesting at birth. Most patients die in the first weeks of life. In this work, we present 3 patients with SMA type 0 who survived >1 year and presented diffuse and progressive brain abnormalities on magnetic resonance imaging, which are not usually seen in patients with SMA. Thus, severe brain involvement may likely be the full end manifestation of an already extreme SMA phenotype caused by substantial reduction of the SMN protein in the brain. ANN NEUROL 2019
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Artigos e Materiais de Revistas Científicas - FM/MNE
Departamento de Neurologia - FM/MNE

Artigos e Materiais de Revistas Científicas - HC/ICHC
Instituto Central - HC/ICHC

Artigos e Materiais de Revistas Científicas - LIM/03
LIM/03 - Laboratório de Medicina Laboratorial

Artigos e Materiais de Revistas Científicas - LIM/15
LIM/15 - Laboratório de Investigação em Neurologia

Artigos e Materiais de Revistas Científicas - LIM/45
LIM/45 - Laboratório de Fisiopatologia Neurocirúrgica


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