频谱障碍:一个未被认可和复杂的神经代谢障碍组
Paulo Sgobbi1, Igor Braga Farias1, Paulo de Lima Serrano1
1Division of Neuromuscular Diseases, Neurometabolic Unit, Division of Neuromuscular Diseases, Federal University of São Paulo (UNIFESP), São Paulo 04039-060, SP, Brazil.
一种罕见的遗传性疾病,PNPT1相关的性动脉,导致渐进的性,动脉和视力丧失. 基因检测发现了PNPT1基因变异,这对于诊断这种疾病至关重要.
科学领域:
- 遗传学 是一个遗传学.
- 神经学 神经学
- 眼科医生 眼科 眼科
背景情况:
- 性动力衰竭和性是复杂的神经系统疾病.
- 光学缩和认知衰退可能是相关的特征.
- 遗传病因是多样化的,包括遗传性性和脊髓小脑动症.
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