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1. The patient's conditionwas diagnosed as pigmentary degeneration ofthe corpus callosum, whichis a rare neurological disorder.
患者的病情被诊断为胼胝体色素变性,这是一种罕见的神经性疾病。
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2. The patient's family history revealedthat they had a relative withpigmentary degeneration of the corpus callosum, indicating a geneticpredisposition.
患者的家族病史显示,他们有一个亲戚患有胼胝体色素变性,这表明存在遗传倾向。
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3. The patient's cognitive function began to decline after thediagnosis of pigmentary degeneration of thecorpus callosum, leading tosignificant difficulties in daily activities.
在诊断出胼胝体色素变性后,患者的认知功能开始下降,导致日常生活出现显著困难。