نتایج جستجو برای: congenital anomaly

تعداد نتایج: 151428  

Journal: :Circulation. Cardiovascular genetics 2011
Alex V Postma Klaartje van Engelen Judith van de Meerakker Thahira Rahman Susanne Probst Marieke J H Baars Ulrike Bauer Thomas Pickardt Silke R Sperling Felix Berger Antoon F M Moorman Barbara J M Mulder Ludwig Thierfelder Bernard Keavney Judith Goodship Sabine Klaassen

BACKGROUND Ebstein anomaly is a rare congenital heart malformation characterized by adherence of the septal and posterior leaflets of the tricuspid valve to the underlying myocardium. An association between Ebstein anomaly with left ventricular noncompaction (LVNC) and mutations in MYH7 encoding β-myosin heavy chain has been shown; in this report, we have screened for MYH7 mutations in a cohort...

Introduction: Orofacial clefts are among the most common congenital anomalies. Patients presenting with orofacial clefts often require surgery or other complex procedures. A cleft lip or palate can be a single anomaly or a part of multiple congenital anomalies. The reported prevalence of cleft disease and associated anomalies varies widely across the literature, and is dependent on the diagnost...

Congenital diaphragmatic hernia (CDH) is a rare congenital anomaly of the diaphragm with an incidence of 1:2000-5000 of live births. This study retrospectively evaluated patients who had been operated on for CDH at our department of Pediatric Surgery between January 2013 and December 2016. The Demographic Data and outcomes of right CDH cases (Group 1) were compared with left CDH cases (Group 2).

Journal: :iranian journal of otorhinolaryngology 0
shahin abdollahi fakhim department of otorhinolaryngology head and neck surgery, tabriz university of medical sciences, tabriz, iran. nikzad shahidi department of otorhinolaryngology head and neck surgery, tabriz university of medical sciences, tabriz, iran. alireza lotfi department of otorhinolaryngology head and neck surgery, tabriz university of medical sciences, tabriz, iran.

introduction: orofacial clefts are among the most common congenital anomalies. patients presenting with orofacial clefts often require surgery or other complex procedures. a cleft lip or palate can be a single anomaly or a part of multiple congenital anomalies. the reported prevalence of cleft disease and associated anomalies varies widely across the literature, and is dependent on the diagnost...

Journal: :JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH 2017

Journal: :Ear, Nose & Throat Journal 2000

Journal: :journal of comprehensive pediatrics 0
saleheh ala department of pediatrics, hamadan university of medical sciences, hamadan, ir iran mahmood haghighat department of pediatrics, shiraz university of medical sciences, shiraz, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی همدان (hamadan university of medical sciences) seyed mohsen dehghani department of pediatrics, shiraz university of medical sciences, shiraz, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences) karmella kamali department of radiology, shiraz university of medical sciences, shiraz, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences) hassan bazmamoun department of pediatrics, hamadan university of medical sciences, hamadan, ir iran; department of pediatrics, hamadan university of medical sciences, hamadan, ir iran. tel: +98-9121331917, fax: +98-8112667766سازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences)

introduction congenital microgastria is an extremely rare anomaly, which is due to failure of gastric development, and causes a tubular stomach with reduced capacity. it is almost always associated with other congenital anomalies. case presentation the patient was a two-month-old boy with microgastria in association with gastroesophageal reflux, tracheomalacia, and limb defect. discussion most ...

Journal: :Proceedings of the Royal Society of Medicine 1913

N NEZAKATGOO, SA MALEK HOSSEINI,

Congenital broncho-esophageal fistula (BEF) is a rare anomaly usually detected in adulthood. In one of the latest reviews of this anomaly, no more than 150 cases were found in the world literature. We report our experience with a 49 year old male patient referring with a classic presentation of chronic cough and choking episodes upon liquid intake. Broncho-esophageal fistula was confirmed b...

2015
S. Liu J. Rouleau J. A. León R. Sauve K. S. Joseph

Objective: To examine the impact of pre-pregnancy diabetes mellitus (DM) on the population birth prevalence of congenital anomalies in Canada. Methods: We carried out a population-based study of all women who delivered in Canadian hospitals (except those in the province of Quebec) between April 2002 and March 2013 and their live-born infants with a birth weight of 500 grams or more and/or a ges...

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