神经系统遗传病课后思考题

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回答

by BARAL BIDUSHA 2017临床医学(中国政府奖学金) -
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1. Trinucleotide repeat amplification ,ion channel disease, genetic metabolic disease, abnormal protein product deposition , metal ion transport disorder.

2.Friedreich type ataxia is the most common autosomal recessive disorder. Spinocerebellar ataxia included SCAI-SCA29,SCA9 unknown, SA24 autosomal recessive inheritance and X-linked recessive heredity were rare.

The main genetic mode of peroneal muscular dystrophy is autosomal dominant inheritance.