CONTENTS

Karyotype Analysis/Genetic Testing in Children Suspected with Hereditary Disease 

  • ZENG Fan-yong ,
  • LIU Jian-jun ,
  • ZHANG Yan ,
  • LI Nan-ling
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  • 1. Capital Medical University School of Rehabilitation Medicine, Beijing 100068, China;
    2. Beijing Bo'ai Hospital, China Rehabilitation Research Centre, Beijing 100068, China

Received date: 2016-11-08

  Revised date: 2017-03-19

  Online published: 2017-08-24

Abstract

Objective To apply karyotype analysis/genetic testing in children suspected with hereditary disease. Methods From July, 2014 to July, 2016, a total of 47 cases in our department were tested using G-banding karyotype analysis or selected the relevant genetic package, for screening the related diseases. Results 38 cases received karyotype analysis, in which three cases were abnormal, and one case was diagnosed definitely. And nine cases received related genetic testing, in which seven cases were abnormal, and four cases were diagnosed definitely. Totally, the positive rate was 21.28%, and the diagnosis rate was 10.64%. Conclusion Karyotype analysis/genetic testing is an etiological diagnosis method for highly suspected hereditary disease in children.

Cite this article

ZENG Fan-yong , LIU Jian-jun , ZHANG Yan , LI Nan-ling . Karyotype Analysis/Genetic Testing in Children Suspected with Hereditary Disease [J]. Chinese Journal of Rehabilitation Theory and Practice, 2017 , 23(8) : 965 -970 . DOI: 10.3969/j.issn.1006-9771.2017.08.020

References

[1] 边旭明.实用产前诊断学[M]. 北京:人民军医出版社, 2008: 496-506.
[2] 钱欣,王建莉. 遗传性疾病产前诊断方法及其进展[J]. 中国产前诊断杂志(电子版), 2014, 6(3): 49-53.
[3] Hulten MA, Dhanjal S, Pertl B. Rapid and simple prenatal diagnosis of common chromosome disorders: advantages and disadvantages of the molecular methods FISH and QF-PCR [J]. Reproduction, 2003, 126(3): 279-297.
[4] Van Karnebeek CD, Jansweijer MC, Leenders AG, et al. Diagnostic investigations in individuals with mental retardation: a systematic literature review of their usefulness [J]. Eur J Hum Genet, 2005, 13(1): 6-25.
[5] Stankiewicz P, Beaudet AL. Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation [J]. Curr Opin Genet Dev, 2007, 17(3): 182-192.
[6] Koolen DA, Pfundt R, de Leeuw N, et al. Genomic microarrays in mental retardation: a practical workflow for diagnostic applications [J]. Hum Mutat, 2009, 30(3): 283-292.
[7] Wessendorf S, Fritz B, Wrobel G, et al. Automated screening for genomic imbalances using matrixbased comparative genomic hybridization [J]. Lab Invest, 2002, 82(1): 47-60.
[8] Chen M, Yang YS, Shih JC, et al. Microdeletions/duplications involving TBXl gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in-situ hybridization [J]. Ultrasound Obstet Gynecol, 2014, 43(4): 396-403.
[9] Torti EE, Braddock SR, Bemreuter K, et al. Oculo-auriculo-vertebral spectrum, cat eye, and distal 22q11 microdeletion syndromes: a unique double rearrangement [J]. Am J Med Genet A, 2013, 161(8): 1992-1998.
[10] Sadr-Nabavi A, Saeidi M. Chromosome duplication (14q) and the genotype phenotype correlation [J]. Int J Fertil Steril, 2014, 8(1): 95-98.
[11] Cain CC, Saul DO, Oehler E, et al. Prenatal detection of a subtle unbalanced chromosome rearrangement by karyotyping,FISH and array comparative genomic hybridization [J]. Fetal Diagn Ther, 2008, 24(3): 286-290.
[12] Costa JL, Meijer G, Ylstra B, et al. Array comparative genomic hybridization copy number profiling: a new tool for translational research in solid malignancies [J]. Semin Radiat Oncol, 2008, 18(2): 98-104.
[13] Luo J, Balkin N, Stewart JF, et al. Neural tube defects and the 13q deletion syndrome: evidence for a critical region in 13q33-34 [J]. Am J Med Genet, 2000, 91(3): 227-230.
[14] Feenstra I, Vissers LELM, Orsel M, et al. Genotype-phenotype mapping of chromosome 18q deletions by high-resolution array CGH: An update of the phenotypic map [J]. Am J Med Genet Part A, 2007, 143A(16): 1858-1867.
[15] Ignatia BV, Beaudet AL. Comparative genomic hybridization and prenatal diagnosis [J]. Curr Opin Obstet Gynecol, 2006, 18(2): 185-191.
[16] Professional Practice and Guidelines Committee. Manning M, Hudgins L. Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities [J]. Genet Med, 2010, 12(11): 742-745.
[17] 王珺,王立文,陈晓丽,等.不明原因精神发育迟滞/迟缓患儿染色体微失衡致病性分析[J]. 中华实用儿科临床杂志, 2016, 31(17): 1343-1346.
[18] Choolani M, Ho SS, Razvi K, et al. FastFISH: technique for ultrarapid fluorescence in situ hybridization on uncultured amniocytes yielding results within 2h of amniocentesis [J]. Mol Hum Reprod, 2007, 13(6): 355-359.
[19] Precone V, Monaco VD, Esposito MV, et al. Cracking the code of human diseases using next-generation sequencing: applications, challenges, and perspectives [J]. Biomed Res Int, 2015, 2015: 161648.
[20] Wang Z, Liu X, Yang BZ, et al. The role and challenges of exome sequencing in studies of human diseases [J]. Front Genet, 2013, 4: 160.
[21] deVries BB, White SM, Knight SJ, et al. Clinical studies on submicroscopic subtelomeric rearrangements: a checklist [J]. J Med Genet, 2001, 38(3): 145-150.
[22] 王影,何玺玉. 基因芯片在不明原因智力发育障碍的诊断进展[J]. 国际儿科学杂志, 2014, 41(1): 38-40.
[23] 高晶,杨尧,吴虹林,等. 不明原因智力低下/脑发育迟滞患儿的拷贝数变异研究[J]. 中华实用儿科临床杂志, 2016, 31(20): 1550-1555.
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