Choline Kinase Beta–Related Muscular Dystrophy, Appearance of Muscle Involvement on Magnetic Resonance Imaging

• Published in: Pediatric neurology Vol. 54; pp. 49 - 54
• Main Authors: De Goede, Christian, FRCPCH FRCP Edin, Oh, Teik, FRCR, Joseph, Jacob, FRCPath, Muntoni, Francesco, MD, Sewry, Caroline, PhD, FRCPath, Phadke, Rahul, MD, FRCPath
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.01.2016
• Subjects: Child; Choline Kinase - genetics; choline kinase beta; Diagnosis, Differential; Humans; learning difficulties; Leg - pathology; Magnetic Resonance Imaging - methods; Male; mitochondria; muscle MRI; Muscle, Skeletal - pathology; Muscular Dystrophies - diagnosis; Muscular Dystrophies - enzymology; Muscular Dystrophies - genetics; Muscular Dystrophies - pathology; muscular dystrophy; Neurology; Pediatrics; muscular dystrophy; learning difficulties; muscle MRI; choline kinase beta; mitochondria
• ISSN: 0887-8994; 1873-5150
• DOI: 10.1016/j.pediatrneurol.2015.09.018

Abstract Background Clinical presentation with motor delay, proximal weakness, and learning difficulties raise the possibility of a dystrophinopathy, dystroglycanopathy, or myotonic dystrophy. This differential should also include the more recently described choline kinase beta–related muscular dystrophy. This condition is typically characterized by large and abnormally distributed mitochondria on muscle biopsy, which can distinguish this condition from the other muscle conditions in the differential. Methods We present a boy with choline kinase beta mutations with relatively mild clinical manifestations, including proximal weakness, learning difficulties and elevated creatine kinase. Investigations included muscle magnetic resonance imaging (MRI) with T1 axial sequences through thigh and calves, and needle muscle biopsy of the left vastus lateralis muscle. Results MRI showed involvement mainly of the quadriceps femoris, sartorius, and adductor magnus, with selective sparing of the gracilis, hamstrings, and adductor longus and brevis. Muscle biopsy revealed chronic dystrophic features. Oxidative stains demonstrated enlarged mitochondria accentuated peripherally or present diffusely in a few fibres giving a coarsely stippled appearance. A homozygous C.722A>G (p.Asn241Ser) mutation was detected in exon 6 of the CHKB gene. Conclusion This selective pattern of skeletal muscle involvement might be helpful for identifying other patients with this condition, even in the absence of diagnostic muscle pathology.