Lamont P J, Thorburn D R, Fabian V, Vajsar J, Hawkins C, Saada Reisch A, Durling H, Laing N G, Nevo Y
Neurogenetic Unit, Department of Neurology, Royal Perth Hospital, Perth, Western Australia.
Neuropediatrics. 2004 Oct;35(5):302-6. doi: 10.1055/s-2004-821243.
Three infants are described who had nemaline rods on muscle biopsy and isolated deficiency of complex I of the respiratory chain on biochemical analysis. They all manifested failure to thrive from birth, and hypotonia and muscle weakness within the first three months of life. Different genetic defects leading to isolated complex I deficiency have been described associated with a variety of morphological changes on muscle biopsy, but rods have not been described. Nemaline rods have been secondary phenomena in a number of conditions, as well as being the primary abnormality in nemaline myopathy. However, the combination of nemaline rods and complex I deficiency is an association not previously reported.
本文描述了三名婴儿,他们的肌肉活检显示有杆状体肌病,生化分析显示呼吸链复合体I单独缺乏。他们均自出生起就出现生长发育迟缓,在出生后的头三个月内出现肌张力减退和肌肉无力。导致单独复合体I缺乏的不同基因缺陷已被描述与肌肉活检中的多种形态学变化相关,但杆状体肌病此前尚未见报道。杆状体肌病在许多情况下是继发现象,也是杆状体肌病的主要异常表现。然而,杆状体肌病与复合体I缺乏的组合是此前未报道过的关联。