Nemours Biomedical Research, Alfred I. duPont Hospital for Children, Wilmington, Delaware.
Am J Med Genet A. 2013 Dec;161A(12):3042-8. doi: 10.1002/ajmg.a.36154. Epub 2013 Aug 16.
The Escobar variant of multiple pterygium syndrome (OMIM #265000) is a rare, autosomal recessive disorder associated with mutations in the γ-subunit of the nicotinic acetylcholine receptor (CHRNG). CHRNG is expressed in fetal muscle during motor development and contributes to the formation of neuromuscular junctions (NMJs). Anomalies in NMJ structure and function have not been investigated in patients with Escobar syndrome. We report five patients identified as having Escobar syndrome, from four families. In three families, the same mutation (c.459dupA) was identified in CHRNG. A biopsy from brachioradialis muscle was collected from a patient from one of these families and analyzed for NMJ organization using fluorescence microscopy. Compared to spinalis muscle from control patients with idiopathic scoliosis or cerebral palsy (CP), the patient with Escobar syndrome had a significantly higher degree of acetylcholine receptor present outside acetylcholinesterase and significantly less acetylcholinesterase outside acetylcholine receptors. Given the role of the acetylcholine receptor γ-subunit in fetal neuromuscular signal transduction and in establishing the primary encounter of muscle and motor nerve terminal, the CHRNG mutations described in Escobar syndrome may cause a broader disruption of postsynaptic proteins and result in aberrant development of the NMJ due to impaired prenatal neuromuscular transmission and/or abnormal neuromuscular synaptogenesis.
埃斯科瓦尔型多发性翼状胬肉综合征(OMIM#265000)是一种罕见的常染色体隐性疾病,与烟碱型乙酰胆碱受体(CHRNG)的γ亚单位突变有关。CHRNG 在运动发育过程中胎儿肌肉中表达,并有助于形成神经肌肉接头(NMJ)。埃斯科瓦尔综合征患者的 NMJ 结构和功能异常尚未得到研究。我们报道了来自四个家族的五名被确定为患有埃斯科瓦尔综合征的患者。在三个家族中,CHRNG 中发现了相同的突变(c.459dupA)。从这些家族之一的患者收集肱桡肌的活检组织,并使用荧光显微镜分析 NMJ 组织。与特发性脊柱侧凸或脑瘫(CP)患者的脊柱肌相比,埃斯科瓦尔综合征患者的乙酰胆碱受体在乙酰胆碱酯酶外的存在程度显著更高,而乙酰胆碱酯酶在外的乙酰胆碱受体明显减少。鉴于乙酰胆碱受体γ亚单位在胎儿神经肌肉信号转导中的作用以及在肌肉和运动神经末梢的初次接触中建立的作用,埃斯科瓦尔综合征中描述的 CHRNG 突变可能导致突触后蛋白的广泛破坏,并由于产前神经肌肉传递受损和/或异常神经肌肉突触发生而导致 NMJ 发育异常。