Literature DB >> 10998453

Patent ductus arteriosus and microdeletion 22q11 in a patient with Klinefelter syndrome.

G V Velagaleti1, A Kumar, L H Lockhart, R Matalon.   

Abstract

We describe an uncommon association of deletion 22q11 in a patient with Klinefelter syndrome. Even though congenital heart defects (CHD) are not associated with Klinefelter syndrome, further investigation of this patient with patent ductus arteriosus showed a microdeletion of chromosome 22q11.2. While this finding may be coincidental, it is important to further evaluate patients when the clinical features are suggestive of a secondary abnormality.

Entities:  

Mesh:

Year:  2000        PMID: 10998453     DOI: 10.1016/s0003-3995(00)01013-3

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


  2 in total

1.  Phenotypic modifications of patients with full chromosome aneuploidies and concurrent suspected or confirmed second diagnoses.

Authors:  Yuri A Zarate; Katherine A Bosanko; Elizabeth Bhoj; Rebecca Ganetzky; Lois J Starr; Elaine H Zackai; G Bradley Schaefer
Journal:  Am J Med Genet A       Date:  2015-04-25       Impact factor: 2.802

2.  Atypical Association of Angelman Syndrome and Klinefelter Syndrome in a Boy with 47,XXY Karyotype and Deletion 15q11.2-q13.

Authors:  Javier Sánchez; Ana Peciña; Olga Alonso-Luengo; Antonio González-Meneses; Rocío Vázquez; Guillermo Antiñolo; Salud Borrego
Journal:  Case Rep Genet       Date:  2014-10-14
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.