Clinical Genetics and Dysmorphology: Our Extraordinary Experiences.

Author:

Abstract

Abstract Background: We have previously described our extensive experiences with clinical genetic and dysmorphology in a plethora of publications. In a previous study, we reported 43 children with uncommon, rare and very rare genetic and hereditary disorders whom were observed during three-year period (2016-2018). In that series, very rare genetic, the case number 104 of Sanjad-Sakati-Richardson-Kirk syndrome in the world, the case number 130 of Townes Brocks syndrome and the case number 170 of Coffin Siris syndrome in the world. The aim of this paper is to describe our 2019 extraordinary new experiences with genetic disorders and dysmorphic syndromes. Material and methods: During the year 2019, 37 patients (25 males and 12 female) with genetic disorders and dysmorphic syndromes and were studied at the Children Teaching Hospital of Baghdad Medical City. Their ages ranged from 2 days to sixteen years. Results: Eight patients had Down syndrome (6 boys and 2 girls), 5 patients had Cornelia De Lang syndrome (4 boys and one girl), 2 male patients had Fragile X-syndrome, 2 male patients with Prader Willi syndrome, two patients had Noonan syndrome (a boy and girl), 2 brothers had Goldberg Shprintzen syndrome. Ten patients each had Facioscapulohumeral muscular dystrophy, Virchow Seckel Syndrome, Mowat Wilson syndrome, Toriello-Carey Syndrome, Ruprecht Majewski-Bosma syndrome, congenital myotonic muscular dystrophy (Congenital dystrophia myotonica), extended Michelin tire baby, Congenital absent radii without thumb aplasia, Dandy walker syndrome and the syndrome of congenital facial palsy and unilateral anotia. In addition, six children patients had newly recognized syndromes (five boys and one girl). Many of the patients in this series were previously described or reported. Conclusion: This one-year Iraqi pioneering experience in the fields of clinical genetics and clinical dysmorphology should herald the end of the Dark Age in these fields in Iraq.

Publisher

SunKrist Publishing

Reference49 articles.

1. 1. Al-Mosawi AJ. Rare genetic disorders in Iraq. (Ed). LAP Lambert Academic Publishing; Germany. 2011.

2. 2. Al-Mosawi AJ. Down syndrome Atlas. (Ed). LAP Lambert Academic Publishing; Germany. 2018.

3. 3. Al-Mosawi AJ. Dramatic effect of non-17 alpha alkyl testosterone derivative anabolic agent on growth in a child with achondroplasia on the short term. Therapy (London). 2006: 3: 605-607.

4. 4. Al-Mosawi AJ. Oculo-cerebro-renal syndrome phenotype in four Iraqi children. Journal of Pediatric Neurology. 2007; 5: 75-78.

5. 5. Al-Mosawi AJ. Nephropathic cystinosis in Iraqi children. The N Iraqi J Med. 2006; 2: 22-25.

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Advancing Clinical Genetics Diagnostic Skills: Cherubism.;Global Journal of Surgery and Surgical Techniques;2021-03-01

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3