Unambiguous molecular detections with multiple genetic approach for the complicated chromosome 22q11 deletion syndrome

Chen Yang, Cheng Hung Huang, Mei Leng Cheong, Kun Long Hung, Lung Huang Lin, Yeong Seng Yu, Chih Cheng Chien, Huei Chen Huang, Chan Wei Chen, Chi Jung Huang

研究成果: 雜誌貢獻文章同行評審

10 引文 斯高帕斯(Scopus)


Background: Chromosome 22q11 deletion syndrome (22q11DS) causes a developmental disorder during the embryonic stage, usually because of hemizygous deletions. The clinical pictures of patients with 22q11DS vary because of polymorphisms: on average, approximately 93% of affected individuals have a de novo deletion of 22q11, and the rest have inherited the same deletion from a parent. Methods using multiple genetic markers are thus important for the accurate detection of these microdeletions. Methods: We studied 12 babies suspected to carry 22q11DS and 18 age-matched healthy controls from unrelated Taiwanese families. We determined genomic variance using microarray-based comparative genomic hybridization (array-CGH), quantitative real-time polymerase chain reaction (qPCR) and multiplex ligation-dependent probe amplification (MLPA). Results: Changes in genomic copy number were significantly associated with clinical manifestations for the classical criteria of 22q11DS using MPLA and qPCR (p < 0.01). An identical deletion was shown in three affected infants by MLPA. These reduced DNA dosages were also obtained partially using array-CGH and confirmed by qPCR but with some differences in deletion size. Conclusion: Both MLPA and qPCR could produce a clearly defined range of deleted genomic DNA, whereas there must be a deleted genome that is not distinguishable using MLPA. These data demonstrate that such multiple genetic approaches are necessary for the unambiguous molecular detection of these types of complicated genomic syndromes.

期刊BMC Medical Genetics
出版狀態已發佈 - 2009

ASJC Scopus subject areas

  • 遺傳學
  • 遺傳學(臨床)


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