Vuopala K, Pedrosa-Domellöf F, Herva R, Leisti J, Thornell L E
Department of Clinical Genetics, University of Oulu, Finland.
Acta Neuropathol. 1995;90(2):176-83. doi: 10.1007/BF00294318.
Two female siblings with the fetal akinesia deformation sequence (FADS) are described. Both showed facial anomalies, arthrogrypotic extremities, hypoplastic lungs, and fetal growth retardation. The central nervous system of the second sibling, including the spinal cord, was normal. The skeletal muscle was studied by immunohistochemistry for the expression of several myosin heavy chain isoforms, M-band proteins and intermediate filament proteins. The skeletal muscle was immature and atypical muscle spindles containing up to 31 intrafusal fibers were found. These findings suggest that a lethal FADS phenotype may involve a maturation defect of the skeletal muscle, and, in this family, may be inherited in a recessive fashion.
本文描述了两名患有胎儿运动不能性畸形序列征(FADS)的女性同胞。两人均表现出面部异常、关节挛缩的四肢、肺发育不全和胎儿生长受限。第二名同胞的中枢神经系统,包括脊髓,是正常的。通过免疫组织化学研究骨骼肌中几种肌球蛋白重链同工型、M带蛋白和中间丝蛋白的表达。骨骼肌不成熟,发现了含有多达31条梭内纤维的非典型肌梭。这些发现表明,致死性FADS表型可能涉及骨骼肌的成熟缺陷,并且在这个家族中可能以隐性方式遗传。