Khalil Mohammed Rohi, Laulund Lone Walentin, Aavild Ploug Anna Julie, Elle Ida Coordt, Fenger-Groen Jesper
Department of Gynecology and Obstetrics, Hospital of Lillebaelt, Kolding, Denmark.
HC Andersen Children's and Youth Hospital, Odense University Hospital, Odense, Denmark.
Am J Case Rep. 2025 Apr 23;26:e946839. doi: 10.12659/AJCR.946839.
BACKGROUND Congenital myasthenic syndrome (CMS) is a rare inherited neuromuscular disorder characterized by muscle weakness and fatigue, often presenting at birth or early childhood. The condition arises from mutations affecting the neuromuscular junction, with an incidence of 1.5 to 9 per million. CMS is primarily classified into presynaptic, synaptic, and postsynaptic types, with mutations in the choline acetyltransferase (CHAT) gene responsible for 4% to 5% of cases. The CHAT gene encodes an enzyme vital for acetylcholine synthesis, a neurotransmitter essential for neuromuscular communication. Mutations in CHAT disrupt acetylcholine production, impairing signal transmission at the neuromuscular junction. This report aims to present a rare case of CMS and highlight the significance of early genetic diagnosis and treatment. CASE REPORT We present a rare case of a newborn girl with autosomal recessive CMS caused by compound heterozygous mutations in the CHAT gene: CHAT c.1679A>G and CHAT c.287-1G>C. Born prematurely at 31 weeks gestation, she presented with severe hypotonia, respiratory failure, and absent spontaneous movements. Genetic testing confirmed CMS. Initial treatment with oral pyridostigmine was ineffective, necessitating a switch to intravenous neostigmine, followed by continuous subcutaneous administration. This resulted in significant clinical improvement, including weaning off mechanical ventilation and achieving developmental milestones, with ongoing physiotherapy. CONCLUSIONS This case underscores the importance of early genetic testing in neonates with unexplained muscle weakness and respiratory failure. Early genetic diagnosis and personalized treatment with acetylcholinesterase inhibitors were key to the infant's recovery, highlighting the potential for positive outcomes even in severe CMS cases due to ChAT mutations.
先天性肌无力综合征(CMS)是一种罕见的遗传性神经肌肉疾病,其特征为肌肉无力和疲劳,通常在出生时或幼儿期出现。该病由影响神经肌肉接头的突变引起,发病率为百万分之1.5至9。CMS主要分为突触前型、突触型和突触后型,胆碱乙酰转移酶(CHAT)基因突变导致4%至5%的病例。CHAT基因编码一种对乙酰胆碱合成至关重要的酶,乙酰胆碱是神经肌肉通讯所必需的神经递质。CHAT基因突变会破坏乙酰胆碱的产生,损害神经肌肉接头处的信号传递。本报告旨在介绍一例罕见的CMS病例,并强调早期基因诊断和治疗的重要性。病例报告:我们报告一例罕见的新生儿女孩,患有由CHAT基因复合杂合突变引起的常染色体隐性CMS:CHAT c.1679A>G和CHAT c.287-1G>C。她在妊娠31周时早产,出生时表现为严重肌张力减退、呼吸衰竭和无自主运动。基因检测确诊为CMS。最初口服吡啶斯的明治疗无效,需要改用静脉注射新斯的明,随后持续皮下给药。这导致了显著的临床改善,包括撤机和达到发育里程碑,目前正在进行物理治疗。结论:本病例强调了对不明原因肌肉无力和呼吸衰竭的新生儿进行早期基因检测的重要性。早期基因诊断和使用乙酰胆碱酯酶抑制剂进行个性化治疗是婴儿康复的关键,突出了即使是由ChAT突变引起的严重CMS病例也有取得积极结果的潜力。