Clinical characteristics of a case of multiple mitochondrial dysfunction syndrome 3

• Published in: Molecular genetics & genomic medicine 2024-06, Vol.12 (6), p.e2485-n/a
• Main Authors: Xu, Hai, Ma, Kai, Gao, Yuye, Song, Qijun, Chen, Chaojin, Xu, Xiao, Peng, Jiaxi, Sun, Yan
• Format: Article
• Language: English
• Subjects: Abdomen; acute neurologic regression; Arm; Bioinformatics; Blood; Blood levels; Brain; Carrier Proteins; Corpus callosum; Diagnosis; Female; Genes; Genetic analysis; Genetic counseling; Genetic screening; Genetic testing; Humans; Hypotonia; IBA57; Infant; Laboratory tests; Lactic acid; Language; Leukoencephalopathy; Male; Microfilament Proteins - genetics; Mitochondrial Diseases; multiple mitochondrial dysfunction syndrome (MMDS); Muscle strength; Mutation; Nonsense mutation; Occipital lobes; Original; Phenotype; Phenotypes; Proteins; Sensory integration; Substantia alba; Whole genome sequencing
• ISSN: 2324-9269; 2324-9269
• DOI: 10.1002/mgg3.2485

Objective To further comprehend the phenotype of multiple mitochondrial dysfunction syndrome type 3 (MMDS3:OMIM#615330) caused by IBA57 mutation. We present a case involving a patient who experienced acute neurological regression, and the literature was reviewed. Methods Clinical data and laboratory test results were collected; early language and development progress were tested; and genetic testing was performed. Bioinformatics analysis was performed using Mutation Taster and PolyPhen‐2, and the literature in databases such as PubMed and CNKI was searched using MMDS3 and IBA57 as keywords. Results The child, aged 1 year and 2 months, had motor decline, unable to sit alone, limited right arm movement, hypotonia, hyperreflexia of both knees, and Babinski sign positivity on the right side, accompanied by nystagmus. Blood lactate levels were elevated at 2.50 mmol/L. Brain MR indicated slight swelling in the bilateral frontoparietal and occipital white matter areas and the corpus callosum, with extensive abnormal signals on T1 and T2 images, along with the semioval center and occipital lobes bilaterally. The multiple abnormal signals in the brain suggested metabolic leukoencephalopathy. Whole‐exome sequencing analysis revealed that the child had two heterozygous mutations in the IBA57 gene, c.286T>C (p.Y96H) (likely pathogenic, LP) and c.992T>A (p.L331Q) (variant of uncertain significance, VUS). As of March 2023, a literature search showed that 56 cases of MMDS3 caused by IBA57 mutation had been reported worldwide, with 35 cases reported in China. Among the 35 IBA57 mutations listed in the HGMD database, there were 28 missense or nonsense mutations, 2 splicing mutations, 2 small deletions, and 3 small insertions. Conclusion MMDS3 predominantly manifests in infancy, with primary symptoms including feeding difficulties, neurological functional regression, muscle weakness, with severe cases potentially leading to mortality. Diagnosis is supported by elevated lactate levels, multisystem impairment (including auditory and visual systems), and distinctive MRI findings. Whole‐exome sequencing is crucial for diagnosis. Currently, cocktail therapy offers symptomatic relief.