加纳科勒布教学医院的一名 13 岁男孩被诊断​​患有威尔逊氏病，这是一种导致铜过量积累的罕见遗传性疾病。 13-year-old boy in Ghana's Korle Bu Teaching Hospital diagnosed with Wilson's Disease, a rare inherited disorder causing excessive copper accumulation.

加纳科勒布教学医院记录了第一例威尔逊氏病患者，患者是一名 13 岁的男孩。 Ghana's Korle Bu Teaching Hospital records first case of Wilson's Disease in a 13-year-old boy. 这种罕见的遗传性疾病会导致器官中铜过量积累，影响发达国家每 30,000 人中就有 1 人患有此病。 The rare, inherited disorder causes excessive copper accumulation in organs and affects one in 30,000 people in developed countries. 男孩的母亲发现他的笔迹越来越糟糕，于是对其进行了诊断和治疗，但每月 450 加纳塞地的药费让她很担心。 The boy's mother detected deteriorating handwriting, leading to diagnosis and treatment, though cost is a concern with monthly medication at GH¢450.