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1.The child has a rare genetic condition called Mongolian Encephalopathy.
这个孩子患有一种罕见的遗传性疾病,叫做蒙古症。
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2. The diagnosis of Mongolian Encephalopathy requires a thorough investigation of the patient's medical history and family background.
蒙古症的诊断需要对患者的医疗史和家族背景进行彻底调查。
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3. Treatment for Mongolian Encephalopathy typically involves a combination of medication and lifestylechanges.
治疗蒙古症通常需要药物治疗和生活方式的改变相结合。