Literature DB >> 22687844

Down-Klinefelter syndrome (48,XXY,+21) in a child with congenital heart disease: case report and literature review.

Zheng Shen1, Chao Chun Zou, Shi Qiang Shang, Ke Wen Jiang.   

Abstract

Congenital heart disease (CHD) is extremely rarely reported in 48, XYY, +21 karyotype. Herein, we reported one case of 48,XYY,+21 karyotype with CHD and reviewed the available literature. The phenotypic characteristics of the 4-month-old child showed the presence of features typical of mongoloid slant. X-ray detection showed the form of heart was corpulent and the bilateral mediastinum was broad. Doppler echocardiogram detection showed atrial septal and ventricular septal defects with patent ductus arteriosus, pulmonary hypertension and mild tricuspid regurgitation. Including this case, 63 cases of 48, XYY, +21 chromosome pattern have been reported. However, only 9 cases have CHD.

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Year:  2012        PMID: 22687844     DOI: 10.2169/internalmedicine.51.7097

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


  6 in total

1.  Double trisomy 48,XXX,+18 with multiple dysmorphic features.

Authors:  Zi-Yan Jiang; Xiao-Hui Wu; Chao-Chun Zou
Journal:  World J Pediatr       Date:  2015-01-28       Impact factor: 2.764

2.  A Rare Double Aneuploidy Case (Down-Klinefelter).

Authors:  Sevcan Tug Bozdogan; Atil Bisgin
Journal:  J Pediatr Genet       Date:  2017-07-06

Review 3.  Klinefelter syndrome: cardiovascular abnormalities and metabolic disorders.

Authors:  A E Calogero; V A Giagulli; L M Mongioì; V Triggiani; A F Radicioni; E A Jannini; D Pasquali
Journal:  J Endocrinol Invest       Date:  2017-03-03       Impact factor: 4.256

4.  Down-Klinefelter Syndrome (48,XXY,+21) in a Saudi Neonate: A Case Report and Literature Review.

Authors:  Jubara Alallah; Sohaib Habhab; Farzeen Mohtisham; Aiman Shawli; Mustafa Daghistani
Journal:  Cureus       Date:  2022-04-28

5.  Double Aneuploidy 48,XXY,+21 Associated with a Congenital Heart Defect in a Neonate.

Authors:  X Shu; C Zou; Z Shen
Journal:  Balkan J Med Genet       Date:  2013-12       Impact factor: 0.519

6.  A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21.

Authors:  Jin Li; Mingshui Xie; Fang Wang; Jianhong Ma; Jiafu Li; Chen Chen; Zhimin Li; Juan Wang; Yuanzhen Zhang; Yirong Li
Journal:  Mol Genet Genomic Med       Date:  2020-05-28       Impact factor: 2.183

  6 in total

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