被诊断为精神分裂症的患者和他们的亲生父母是否同时出现马凡氏综合征的症状?横断面研究

IF 0.2 Q4 PSYCHIATRY Annals of Indian Psychiatry Pub Date : 2023-01-01 DOI:10.4103/aip.aip_131_22
Kuldeep Saneja, Devavrat G. Harshe, Ankit Halder, N. Ravindran, Gurudas Harshe
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引用次数: 0

摘要

背景:马凡氏综合征(MFS)的患病率为2-3/100000人,而精神分裂症的患病率则为100/10000人。尽管现有文献没有强有力的科学证据支持这种联系,但应该探索这种联系的可能性,因为患有MFS的患者确实比普通人群有更高程度的精神合并症。材料和方法:横断面研究随机招募了50名精神分裂症患者及其亲生父母。所有患者和对照组均接受了临床检查,包括精神状态检查、屈光和裂隙灯检查的眼科评估、骨骼畸形的人体测量评估和二维超声心动图评估。结果:所有患者的上段/下段比例、臂展/高展、裂隙灯检查结果、屈光度和主动脉根Z评分均正常。性别之间、患者和对照组之间的人体测量和Z评分没有显著差异。结论:本研究未发现精神分裂症患者及其亲生父母同时出现马法尼样特征。
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Do patients diagnosed with schizophrenia and their biological parents have concurrent signs suggestive of Marfan's syndrome? A cross sectional study
Background: The prevalence of Marfan's syndrome (MFS) is 2–3/10,000 people, whereas the prevalence of schizophrenia is 100/10,000 people. Although existing literature does not have robust scientific evidence to support such an association, the possibility of such should be explored because patients suffering from MFS do have higher degree of psychiatric comorbidities than the general population. Materials and Methods: The cross-sectional study randomly recruited 50 patients with schizophrenia and both their biological parents. All patients and controls were examined clinically for mental status examination, ophthalmological evaluation with refraction and slit-lamp examination, anthropometric evaluation for skeletal deformities, and two-dimensional echocardiographic assessment. Results: All the patients had a normal upper segment/lower segment ratio, arm span/height span, slit-lamp examination results, refraction, and aortic root Z score. There was no significant difference in anthropometric measurements and Z scores between genders and between patients and control groups. Conclusion: The study found no co-occurrence of marfanoid features in schizophrenic patients and their biological parents.
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自引率
25.00%
发文量
38
审稿时长
23 weeks
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