Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota, USA.
Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota, USA.
Am J Med Genet A. 2023 Jun;191(6):1626-1631. doi: 10.1002/ajmg.a.63179. Epub 2023 Mar 17.
ALG13-CDG is a rare X-linked disorder of N-linked glycosylation. Given the lack of long-term outcome data in ALG13-CDG, we collected natural history data and reviewed individuals surviving to young adulthood with confirmed pathogenic variants in ALG13 in our own cohort and in the literature. From the 14 ALG13-CDG patients enrolled into our Frontiers of Congenital Disorders of Glycosylation Consortium natural history study only two patients were older than 16 years; one of these two females is so far unreported. From the 52 patients described in the medical literature with confirmed pathogenic variants in ALG13 only five patients were older than 16 years (all females), in addition to the new, unreported patient from our natural history study. Two male patients have died due to ALG13-CDG, and there were no surviving males older than 16 years with a confirmed ALG13-CDG diagnosis. Our adolescent and young adult cohort of six patients presented with epilepsy, muscular hypotonia, speech, and developmental delay. Intellectual disability was present in all female patients with ALG13-CDG. Unreported features included ataxia, neuropathy, and severe gastrointestinal symptoms requiring G/J tube placement. In addition, two patients from our natural history study developed unilateral hearing loss. Skeletal abnormalities were found in four patients, including osteopenia and scoliosis. Major health problems included persistent seizures in three patients. Ketogenic diet was efficient for seizures in three out of four patients. Although all patients were mobile, they all had severe communication problems with mostly absent speech and were unable to function without parental support. In summary, long-term outcome in ALG13-CDG includes gastrointestinal and skeletal involvement in addition to a chronic, mostly non-progressive neurologic phenotype.
ALG13-CDG 是一种罕见的 X 连锁 N-连接糖基化缺陷病。鉴于缺乏 ALG13-CDG 的长期结局数据,我们在自身队列和文献中收集了确诊为 ALG13 致病性变异的个体存活至成年早期的自然病史数据。在我们的先天性糖基化障碍前沿研究协会的自然病史研究中,仅纳入了 14 名 ALG13-CDG 患者,其中只有两名患者年龄大于 16 岁;这两名患者中,有一名女性患者此前尚未报道过。在文献中描述的 52 名确诊为 ALG13 致病性变异的患者中,仅有 5 名患者年龄大于 16 岁(均为女性),除此之外,还有一名来自我们自然病史研究的新的、未报道过的患者。两名男性患者因 ALG13-CDG 死亡,且没有确诊为 ALG13-CDG 的存活男性年龄大于 16 岁。我们的青少年和成年患者队列有 6 名患者存在癫痫、肌肉张力减退、言语和发育迟缓。所有女性 ALG13-CDG 患者均存在智力障碍。未报道的特征包括共济失调、周围神经病和需要放置胃空肠造口管的严重胃肠道症状。此外,我们的自然病史研究中有两名患者出现单侧听力损失。4 名患者存在骨骼异常,包括骨质疏松和脊柱侧凸。主要健康问题包括 3 名患者持续性癫痫发作。 ketogenic 饮食对 4 名患者中的 3 名患者的癫痫发作有效。尽管所有患者均能移动,但他们都存在严重的沟通问题,多数患者言语缺失,且无法在没有父母支持的情况下生活。总之,ALG13-CDG 的长期结局包括胃肠道和骨骼受累,以及慢性、大多非进行性的神经表型。