DDOST‐CDG: Clinical and molecular characterization of a third patient with a milder and a predominantly movement disorder phenotype. Issue 1 (17th October 2022)

• Record Type: Journal Article
• Authors: Elsharkawi, Ibrahim; Wongkittichote, Parith; Daniel, Earnest James Paul; Starosta, Rodrigo Tzovenos; Ueda, Keisuke; Ng, Bobby G.; Freeze, Hudson H.; He, Miao; Shinawi, Marwan
• Is Part Of: Journal of inherited metabolic disease. Volume 46:Issue 1(2023)
• Page Start: 92
• Page End: 100
• Publication Date: 2022-10-17
• Subjects: congenital disorders of glycosylation -- movement disorders -- N‐glycans -- tremor -- type I CDG; Metabolism, Inborn errors of -- Periodicals; Metabolism -- Disorders -- Periodicals; 616.39042
• DOI: 10.1002/jimd.12565
• Languages: English
• ISSNs: 0141-8955

Abstract

Abstract: Congenital disorders of glycosylation (CDG) are a group of heterogeneous inherited metabolic disorders affecting posttranslational protein modification. DDOST‐CDG, caused by biallelic pathogenic variants in DDOST which encodes dolichyl‐diphospho‐oligosaccharide‐protein glycosyltransferase, a subunit of N‐glycosylation oligosaccharyltransferase (OST) complex, is an ultra‐rare condition that has been described in two patients only. The main clinical features in the two reported patients include profound developmental delay, failure to thrive, and hypotonia. In addition, both patients had abnormal transferrin glycosylation. Here, we report an 18‐year‐old male who presented with moderate developmental delay, progressive opsoclonus, myoclonus, ataxia, tremor, and dystonia. Biochemical studies by carbohydrate deficient transferrin analysis showed a type I CDG pattern. Exome sequencing identified compound heterozygous variants in DDOST : a maternally inherited variant, c.1142dupT (p.Leu381Phefs*11), and a paternally inherited variant, c.661 T > C (p.Ser221Pro). Plasma N‐glycan profiling showed mildly increased small high mannose glycans including Man0‐5 GlcNAc2, a pattern consistent with what was previously reported in DDOST‐CDG or defects in other subunits of OST complex. Western blot analysis on patient's fibroblasts revealed decreased expression of DDOST and reduced intracellular N‐glycosylation, as evident by the biomarkers ICAM‐1 and LAMP2. Our study highlights the clinical variability, expands the clinical and biochemical phenotypes, and describes new genotype, which all are essential for diagnosing and managing patients with DDOST‐CDG. Abstract :