Alzwaihri Abubakr Salem, Almasoudi Eid Ayed, Hadrawi Manal Taha, Danish Enam Y, Alasmari Faisal Fahad, Ahmed Hassan Arafah
Emergency Department, Al Mahani Hospital, Taif City, Saudi Arabia.
College of Medicine, University of Jeddah, Jeddah, Saudi Arabia.
Ann Med Surg (Lond). 2025 Feb 7;87(5):2602-2607. doi: 10.1097/MS9.0000000000003001. eCollection 2025 May.
Cysteine β-synthase deficiency, often known as classic homocystinuria, is an uncommon inborn mistake in methionine metabolism. Developmental delay, intellectual incapacity, skeletal and vascular symptoms, and ocular abnormalities are possible main clinical characteristics.
This study sought to describe the ocular anomalies that King Fahad Armed Forces Hospital, Jeddah, Saudi Arabia, homocystinuria patients presented with between 2018 and 2022.
This retrospective research included six homocystinuria patients. Demographic and clinical characteristics of patients as age, gender, and comorbidities were collected. Relevant clinical and ophthalmic assessments, like visual acuity, fundus examination findings, complications, and type of surgery were also reported.
Six patients with homocystinuria (12 eyes) were included. Associated diseases were mostly mental retardation (100%), epilepsy (66.7%), developmental delay (50.0%), scoliosis (33.3%), bronchiectasis (16.7%), thrombophilia (16.7%), metabolic disorders (16.7%), and deep venous thrombosis (16.7%). All patients had ectopia lentis (100%), while one patient (16.7%) had eye ectropion, one patient (16.7%) had anterior uveitis, and one patient (16.7%) had scleromalacia. Surgery type was mostly lensectomy and vitrectomy (83.3%) then scleral fixation (16.7%), and Grice green procedure (16.7%). There were insignificant differences between first and last Autoref readings in spherical, cylinder, and axis errors of right and left eyes.
Late-diagnosed homocystinuria patients frequently have abnormalities of the eyes. Ectopia lentis should always raise the possibility that homocystinuria is the cause of the condition.
半胱氨酸β-合酶缺乏症,通常被称为经典型同型胱氨酸尿症,是甲硫氨酸代谢中一种罕见的先天性缺陷。发育迟缓、智力障碍、骨骼和血管症状以及眼部异常可能是主要的临床特征。
本研究旨在描述沙特阿拉伯吉达法赫德国王武装部队医院2018年至2022年间同型胱氨酸尿症患者出现的眼部异常情况。
这项回顾性研究纳入了6例同型胱氨酸尿症患者。收集了患者的人口统计学和临床特征,如年龄、性别和合并症。还报告了相关的临床和眼科评估结果,如视力、眼底检查结果、并发症和手术类型。
纳入了6例同型胱氨酸尿症患者(12只眼)。相关疾病主要有智力发育迟缓(100%)、癫痫(66.7%)、发育迟缓(50.0%)、脊柱侧弯(33.3%)、支气管扩张(16.7%)、血栓形成倾向(16.7%)、代谢紊乱(16.