Casado J L, Arenas C, Segura D, Chinchón I, González R, Bautista J
Servicio de Neurología, Hospital Universitario Virgen del Rocío, Sevilla.
Neurologia. 1995 Mar;10(3):145-8.
We present a mother and 2 children with congenital myopathy whose clinical signs were facial paresis in all three, and mild involvement of the lower extremities in the mother and one son. All three presented skeletal abnormalities, hypertelorism, arched palate, retraction of the Achilles tendon or short neck. Symptoms were not progressive and muscle biopsies showed central cores and nemaline rods in the mother and only nemaline rods in the 2 sons. The mother also suffered carpal tunnel syndrome, as had other members of the family as the result of autosomal dominant inheritance.
我们报告了一位母亲和两名患有先天性肌病的儿童,他们三人的临床症状均为面部轻瘫,母亲和其中一个儿子下肢有轻度受累。三人都有骨骼异常、眼距过宽、腭裂、跟腱挛缩或短颈。症状无进行性加重,肌肉活检显示母亲有中央核和杆状体,两名儿子只有杆状体。母亲还患有腕管综合征,该家族其他成员也因常染色体显性遗传患有此病。