Literature DB >> 9036769

Deletions in chromosome 22q11 region in cervical aortic arch.

A Kumar1, J L McCombs, D W Sapire.   

Abstract

Two patients with cervical aortic arch are described, both with deletions in chromosome 22q11 region, and thymic hypofunction. This suggests that cervical aortic arch is part of the spectrum of the CATCH 22 group of defects.

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Year:  1997        PMID: 9036769     DOI: 10.1016/s0002-9149(96)00772-2

Source DB:  PubMed          Journal:  Am J Cardiol        ISSN: 0002-9149            Impact factor:   2.778


  2 in total

1.  Congenital isolation of the subclavian artery in adults.

Authors:  J L Reynolds
Journal:  Tex Heart Inst J       Date:  1997

Review 2.  Aortic arch anomalies, embryology and their relevance in neuro-interventional surgery and stroke: A review.

Authors:  Shilpa S Mantri; Bharath Raju; Fareed Jumah; Michael S Rallo; Anmol Nagaraj; Priyank Khandelwal; Sudipta Roychowdhury; David Kung; Anil Nanda; Gaurav Gupta
Journal:  Interv Neuroradiol       Date:  2021-09-13       Impact factor: 1.764

  2 in total

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