Literature DB >> 2063682

Unusual cardiac malformations in Holt-Oram syndrome: report of two cases.

J M Wu1, M L Young, T R Wang, S J Lin, J K Chang, J Wei.   

Abstract

The Holt-Oram syndrome is a hereditary disease which associated with upper limbs anomalies and cardiac defects such as secundum type atrial septal defect. Two cases of this syndrome with unusual cardiac findings are reported: One has an unroofing coronary sinus type atrial septal defect and preexcitation syndrome, the other has pentalogy of Fallot.

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Year:  1991        PMID: 2063682

Source DB:  PubMed          Journal:  Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi        ISSN: 0001-6578


  1 in total

1.  Syndromic anorectal malformation associated with Holt-Oram syndrome, microcephaly, and bilateral corneal opacity: a case report.

Authors:  Usang E Usang; Thomas U Agan; Akan W Inyang; John-Daniel C Emehute; Itam H Itam
Journal:  J Med Case Rep       Date:  2016-08-05
  1 in total

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