Phanthumchinda K
Department of Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
J Med Assoc Thai. 1992 Jun;75(6):369-73.
The first case of X-linked recessive bulbospinal neuronopathy in a Thai family is described. Clinical features of this entity were discussed. Although two members of this family had classical features of X-linked recessive bulbospinal neuronopathy, there were some differences in distribution of weakness among the affected members. This variation among the members of the affected family was firstly described. The clinical features of this disease especially the associated gynecomastia and essential tremors are distinctive and it is possible to diagnose it even in a sporadic case. Although, the prominent feature of the disease is atrophy and fasciculation of muscles, this entity is not a pure anterior horn cell disorder and should be better classified as a multisystem disorder due to multiple organ involvement.
本文描述了一个泰国家庭中首例X连锁隐性延髓脊髓神经元病病例。讨论了该疾病实体的临床特征。尽管该家族的两名成员具有X连锁隐性延髓脊髓神经元病的典型特征,但受影响成员之间的肌无力分布存在一些差异。首次描述了受影响家族成员之间的这种变异。该疾病的临床特征,尤其是伴发的男性乳房发育和特发性震颤很独特,即使在散发病例中也有可能诊断出来。虽然该疾病的突出特征是肌肉萎缩和肌束震颤,但该疾病实体并非单纯的前角细胞疾病,由于多器官受累,应更好地归类为多系统疾病。