Rodrigues Guilherme G Riccioppo, Walker Ruth H, Brice Alexis, Cazeneuve Cécile, Russaouen Odile, Teive Helio A G, Munhoz Renato Puppi, Becker Nilson, Raskin Salmo, Werneck Lineu Cesar, Junior Wilson Marques, Tumas Vitor
Department of Neurology, Ribeirao Preto School of Medicine, Ribeirao Preto, SP Brazil.
Mov Disord. 2008 Nov 15;23(15):2244-7. doi: 10.1002/mds.22223.
Huntington's disease-like 2 (HDL2) is a neurodegenerative disorder found in people of African ancestry with clinical, radiological, and neuropathological manifestations similar to Huntington's disease (HD). HDL2 is caused by a pathological expansion of CAG/CTG triplets in exon 2A of the JPH3 gene. We describe four cases of HDL2 from four unrelated families, and discuss their clinical findings. HDL2 should be considered in every patient with an HD-like phenotype who tests negative for the HD mutation, even if African ancestry is not immediately apparent.
亨廷顿舞蹈病样2型(HDL2)是一种在非洲裔人群中发现的神经退行性疾病,其临床、影像学和神经病理学表现与亨廷顿舞蹈病(HD)相似。HDL2由JPH3基因外显子2A中CAG/CTG三联体的病理性扩增引起。我们描述了来自四个无关家庭的四例HDL2病例,并讨论了他们的临床发现。对于每一位HD样表型但HD突变检测呈阴性的患者,即使非洲裔血统不明显,也应考虑HDL2的可能性。