نتایج جستجو برای: congenital defect

تعداد نتایج: 207564  

2017
Zeynep Eyileten Adnan Uysalel

Copyright © 2017 Heart and Health Foundation of Turkey (TÜSAV). Published by Medikal Akademi. This article is licensed by Medikal Akademi and TÜSAV under the terms of Creative Commons Attribution License. Eyileten Z., Uysalel A. Isolated ventricular septal defect in infants EJCM 2017; 05 (2): 27-33. Doi: 10.15511/ejcm.17.00227. Ventricular septal defect is a hole in the interventricular septum ...

Journal: :international journal of pediatrics 0
tahereh boryri pregnancy health research center, and school of nursing and midwifery, zahedan university of medical sciences, zahedan, iran. noor mohammad noori children and adolescent health research center, zahedan university of medical sciences, zahedan, iran. alireza teimouri children and adolescent health research center, zahedan university of medical sciences, zahedan, iran. fatemeh sharafi school of medicine, zahedan university of medical sciences, zahedan, iran.

backgroundcongenital heart diseases (chd) are the most common congenital anomaly in children and also the leading cause of mortality from congenital anomalies. various factors including smoking, drinking alcohol and addiction play role in development of congenital heart diseases. this study was conducted with the aim of investigation of the prevalence of addiction in parents of children with co...

Journal: :Medical Journal of Islamic World Academy of Sciences 2016

Journal: :JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH 2016

Journal: :International Medical Case Reports Journal 2016

2010
Anna Wozniak Danuta Wolnik-Brzozowska Marzena Wisniewska Renata Glazar Anna Materna-Kiryluk Tomasz Moszura Magdalena Badura-Stronka Joanna Skolozdrzy Maciej R Krawczynski Joanna Zeyland Waldemar Bobkowski Ryszard Slomski Anna Latos-Bielenska Aldona Siwinska

BACKGROUND The 22q11.2 microdeletion syndrome (22q11.2 deletion syndrome -22q11.2DS) refers to congenital abnormalities, including primarily heart defects and facial dysmorphy, thymic hypoplasia, cleft palate and hypocalcaemia. Microdeletion within chromosomal region 22q11.2 constitutes the molecular basis of this syndrome. The 22q11.2 microdeletion syndrome occurs in 1/4000 births. The aim of ...

Journal: :Orthopedics & Traumatology 1980

Journal: :Collegium antropologicum 2011
Zoran Veir Mladen Duduković Pavle Miklić Davor Mijatović Bruno Cvjeticanin Merica Veir Anto Dujmović

Myelomeningocele is a congenital defect in vertebral arches with cystic dilatation of meninges and structural or functional abnormality of spinal cord or cauda equina. It is a form of spinal dysraphisam with overlying skin defect (spina bifida aperta). That condition is related to other clinical complications such as infection that can produce furthermore complications. To prevent rate of compl...

Journal: :Proceedings of the Royal Society of Medicine 1964

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