Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes with coexisting nemaline myopathy: a case report

• Published in: Journal of medical case reports 2024-09, Vol.18 (1), p.420-7, Article 420
• Main Authors: Gunawardena, Kawmadi, Praveenan, Somasundaram, Dissanayake, Vajira H W, Ratnayake, Pyara
• Format: Article
• Language: English
• Subjects: Acidosis, Lactic - genetics; Arginine; Case Report; Child; DNA sequencing; Epilepsy; Exome Sequencing; Genes; Humans; Lactic acidosis; Levetiracetam; Magnetic Resonance Imaging; Male; Marriage; Medical genetics; MELAS; Mitochondrial Encephalomyopathies - complications; Mitochondrial Encephalomyopathies - diagnosis; Mitochondrial Encephalomyopathies - genetics; Myopathies, Nemaline - complications; Myopathies, Nemaline - genetics; Nemaline myopathy; Nucleotide sequencing; Physical therapy; Sri Lanka; Stroke; Stroke-like episodes; Therapeutics, Physiological
• ISSN: 1752-1947; 1752-1947
• DOI: 10.1186/s13256-024-04723-9

Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes and nemaline myopathy are two rare genetic conditions. We report the first case reported in world literature with coexistence of both these rare disorders. A 11-year-old previously healthy Sri Lankan male child, product of a nonconsanguineous marriage with normal development presented with acute onset short lasting recurring episodes of right-sided eye deviation with impaired consciousness. In between episodes he regained consciousness. Family history revealed a similar presentation in the mother at 36 years of age. Examination was significant for short stature and proximal upper and lower limb weakness. His plasma and cerebrospinal fluid lactate were elevated. Magnetic resonance imaging brain had evidence of an acute infarction in the right occipital territory. Sanger sequencing for common mitochondrial variants of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes confirmed this diagnosis. Whole exome sequencing revealed pathogenic compound heterozygous variants in NEB gene implicating in coexisting nemaline myopathy. Acute presentation was managed with supportive care, antiepileptics, and mitochondrial supplementation. Currently he is stable on daily supplementation of arginine and limb-strengthening physiotherapy. He is being monitored closely clinically and with serum lactate level. Genetic diseases are rare. Coexistence of two genetic conditions is even rarer. Genetic confirmation of diagnosis is imperative for prediction of complications, accurate management, and genetic counseling.