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pro vyhledávání: '"Gregory Chryssostomidis"'
Autor:
Theofili Kousi, Andrew C. Chatzis, Prodromos Azariadis, Vassiliki Fotiadou, Cleo Laskari, Gregory Chryssostomidis, Meletios A. Kanakis, Christos Apostolidis
Publikováno v:
International Journal of Surgery Case Reports
INTRODUCTION The Holt–Oram syndrome is a rare congenital disorder involving the skeletal and cardiovascular systems. It is characterized by upper limb deformities and cardiac malformations, atrial septal defects in particular. PRESENTATION OF CASE