We report a 28-year-old female with known nemaline myopathy who underwent general anesthesia for osteosynthesis of a femoral neck fracture. Preoperative investigations including blood count, urea, serum electrolytes, prothrombin time, partial thromboplastin time, and electrocardiogram were all normal. Pulmonary function studies showed a restrictive defect with normal blood gases. The chest radiograph showed severe scoliosis. Because of the complications reported in nemaline myopathy, e.g. aspiration, hypoventilation, and the unknown predisposition for the development of malignant hyperthermia, we performed "trigger-free" general intubation anesthesia. Anesthesia was induced with propofol 100 mg i.v., nitrous oxide 66%, and oxygen 34%. The cardiac rate, oropharyngeal temperature, and oxygen saturation were recorded continuously. Blood pressure was measured every 5 min. Muscle relaxation was monitored using train-of-four (TOF) stimulation. Atracurium was given intravenously in 5-mg doses until the TOF-ratio was zero, then the patient was intubated and anesthesia maintained by continuous infusion of propofol 0.43 mg/kg per hour. Pulmonary ventilation using a Dräger Sulla 808 was adjusted to keep end-expiratory pCO2 between 32 and 34 mmHg. Fentanyl 0.2 mg was administrated at the beginning of the operation. Fifty minutes after the last bolus of atracurium the TOF-ratio was greater than 75%. At the beginning of skin suturing the propofol infusion was stopped; a few minutes later spontaneous respiration ensued. After extubation emergence was rapid and the patient was fully oriented and awake.(ABSTRACT TRUNCATED AT 250 WORDS)
Download full-text PDF |
Source |
---|
Tunis Med
January 2025
University of Sfax, Military University Hospital of Sfax, Cardiology Department, Sfax, Tunisia.
Introduction: Nemaline myopathy (NM), also known as Nemalinosis, is a rare congenital muscle disease with an incidence of 1 in 50000. It is characterized by nemaline rods in muscle fibers, leading to muscle weakness. We reported a case of NM revealed by cardiac involvement, and we highlighted the challenges in diagnosing this condition as well as its poor prognosis.
View Article and Find Full Text PDFNeurol Genet
February 2025
Department of Medical Genetics, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Canada.
Background And Objectives: Neonatal encephalopathy (NE) is characterized by an abnormal level of consciousness with or without seizures in the neonatal period. It affects 1-6/1,000 live term newborns. We applied genome sequencing (GS) in term newborns with NE to investigate the underlying genetic causes.
View Article and Find Full Text PDFIntroduction: Structural variants (SVs) of the nebulin gene (), including intragenic duplications, deletions, and copy number variation of the triplicate region, are an established cause of recessively inherited nemaline myopathies and related neuromuscular disorders. Large deletions have been shown to cause dominantly inherited distal myopathies. Here we provide an overview of 35 families with muscle disorders caused by such SVs in .
View Article and Find Full Text PDFRes Sq
December 2024
Program for Genetics and Genome Biology, Hospital for Sick Children, Toronto, ON, CAN.
Biallelic pathogenic variants in the nebulin () gene lead to the congenital muscle disease nemaline myopathy. In-frame deletion of exon 55 (ΔExon55) is the most common disease-causing variant in . Previously, a mouse model of was developed; however, it presented an uncharacteristically severe phenotype with a near complete reduction in transcript expression that is not observed in exon 55 patients.
View Article and Find Full Text PDFNeurol India
November 2024
Department of Pathology, All India Institute of Medical Sciences, New Delhi, India.
Sporadic late-onset nemaline rod myopathy is a rare, acquired, sub-acute, adult-onset myopathy characterized by proximal muscle weakness and nemaline rods in the myofibers. In contrast to its congenital form, the prevalence in adult population is comparatively rare. Herein, we report a case of 60-year-old male who presented with insidious onset proximal muscle weakness with myopathic pattern on electromyography.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!