Literature DB >> 16824627

Cardiovascular anomalies in patients with chromosome 22q11.2 deletion: a Korean multicenter study.

In-Sook Park1, Jae-Kon Ko, Young-Hwue Kim, Han-Wook Yoo, Eul-Ju Seo, Jung-Yun Choi, Hong-Yang Gil, Soo-Jin Kim.   

Abstract

BACKGROUND AND OBJECTIVES: The 22q11.2 deletion syndrome is reported with increasing frequency worldwide, and its clinical manifestations, including cardiovascular anomalies, appear to be more diverse than previously reported. The aim of this study was to determine the incidence and the pattern of cardiovascular anomalies in Korean patients with 22q11 deletion.
METHODS: This study involved six Korean institutions. We reviewed the clinical records of patients and confirmed the presence of 22q11.2 deletion by fluorescent in situ hybridization (FISH).
RESULTS: A total of 222 patients were examined and 190 (85.6%) patients had the cardiovascular abnormalities: 63.2% tetralogy of Fallot (TOF), 20.5% isolated ventricular septal defects (VSDs), 5.3% interrupted aortic arch type B (IAA B), 3.6% double outlet right ventricle (DORV), 3.6% atrial septal defects (ASDs) and 1.7% truncus arteriosus (TA). Of 168 patients with VSD, 69.6% had the perimembranous type, 11.9% the total conal defect type, 6.5% the subarterial type, 4.2% the muscular type and 1.2% the mixed type. A right aortic arch was observed in 50% of patients, and an aberrant subclavian artery was significantly more common with a right (30.9%) than a left (18.3%) aortic arch (p<0.05).
CONCLUSIONS: A wide variety of cardiovascular anomalies were present in Korean patients with the 22q11.2 deletion.

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Year:  2006        PMID: 16824627     DOI: 10.1016/j.ijcard.2005.12.029

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN: 0167-5273            Impact factor:   4.164


  8 in total

Review 1.  Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.

Authors:  Marta Unolt; Paolo Versacci; Silvia Anaclerio; Caterina Lambiase; Giulio Calcagni; Matteo Trezzi; Adriano Carotti; Terrence Blaine Crowley; Elaine H Zackai; Elizabeth Goldmuntz; James William Gaynor; Maria Cristina Digilio; Donna M McDonald-McGinn; Bruno Marino
Journal:  Am J Med Genet A       Date:  2018-04-16       Impact factor: 2.802

2.  22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive cases.

Authors:  Shabnam Peyvandi; Philip J Lupo; Jennifer Garbarini; Stacy Woyciechowski; Sharon Edman; Beverly S Emanuel; Laura E Mitchell; Elizabeth Goldmuntz
Journal:  Pediatr Cardiol       Date:  2013-04-21       Impact factor: 1.655

3.  Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease.

Authors:  Wai Lun Alan Fung; Eva W C Chow; Gary D Webb; Michael A Gatzoulis; Anne S Bassett
Journal:  Int J Cardiol       Date:  2008-01-11       Impact factor: 4.164

4.  Clinical and immunophenotypic characteristics of patients with chromosome 22q11.2 deletion syndrome: a single institution's experience.

Authors:  Serdar Nepesov; Fatma Deniz Aygün; Umut Küçüksezer; Emre Taşdemir; Haluk Çokuğraş; Yıldız Camcıoğlu
Journal:  Turk Pediatri Ars       Date:  2019-03-01

5.  Should prenatal chromosomal microarray analysis be offered for isolated ventricular septal defect? A single-center retrospective study from China.

Authors:  Ken Cheng; Hang Zhou; Fang Fu; Tingying Lei; Fucheng Li; Ruibin Huang; You Wang; Xin Yang; Ru Li; Dongzhi Li; Can Liao
Journal:  Front Cardiovasc Med       Date:  2022-09-07

6.  Mosaic 22q11.2 microdeletion syndrome: diagnosis and clinical manifestations of two cases.

Authors:  Ashutosh Halder; Manish Jain; Madhulika Kabra; Neerja Gupta
Journal:  Mol Cytogenet       Date:  2008-08-10       Impact factor: 2.009

7.  Variety of prenatally diagnosed congenital heart disease in 22q11.2 deletion syndrome.

Authors:  Mi-Young Lee; Hye-Sung Won; Ju Won Baek; Jae-Hyun Cho; Jae-Yoon Shim; Pil-Ryang Lee; Ahm Kim
Journal:  Obstet Gynecol Sci       Date:  2014-01-16

8.  The Prevalence of Congenital Heart Diseases in Syndromic Children at King Khalid National Guard Hospital from 2005 to 2016.

Authors:  Elaf M Abduljawad; Ahad AlHarthi; Samah A AlMatrafi; Mawaddah Hussain; Aiman Shawli; Rahaf Waggass
Journal:  Cureus       Date:  2020-04-29
  8 in total

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