Two Brothers With ADSS1 Myopathy: A Report of Clinical, Radiological, and Autopsy Findings

• DOI: 10.1111/neup.70008
• Publication Date: 2025-04-30T07:04:50Z
• Authors: Yuka Hama; Terunori Sano; Yasushi Oya; Chihiro Matsumoto; Yuji Nakayama; Yoshihiko Saito; Aritoshi Iida; Makoto Shibuya; Yuko Saito; Ichizo Nishino; Yuji Takahashi; Masaki Takao

ABSTRACTADSS1 myopathy, previously known as adenylosuccinate synthetase‐like 1 (ADSSL1) myopathy, is an autosomal recessive muscle disease caused by variants in ADSS1 (adenylosuccinate synthase 1). ADSS1 myopathy is complicated by respiratory muscle weakness or cardiomyopathy as well as limb muscle weakness. We analyzed two siblings with ADSS1 myopathy, both harboring compound heterozygous pathogenic variants (c.781G>A/c.919delA) in ADSS1 and provided details of their phenotypes together with muscle imaging and autopsy findings. Although it was reported that ADSS1 myopathy usually began with lower limb muscle weakness, our cases showed early involvement of the cervical paraspinal muscle, triceps brachii muscle, flexor digitorum superficialis and profundus muscles, rectus abdominis muscle, gluteus maximus and medius muscles, and cardiomyopathy. While a previous study reported that the trunk and hip muscles were relatively spared, atrophy of paraspinal muscles, gluteus medius and maximus muscles, and adductor muscles were observed. Our two siblings allowed for long‐term follow‐up and will be useful reference cases. We evaluated the frequency of fibers with nemaline bodies in various autopsied muscles and found that the ratio of fibers with nemaline bodies was lower compared to other nemaline myopathies. Postmortem examination revealed, for the first time, nemaline bodies in the diaphragm and myocardium, associated with respiratory failure and cardiomyopathy.