Background: Infantile hypertrophic pyloric
stenosis affects 0.5 – 3.0 per 1000 live birth and it is
the most common surgical cause of vomiting in
infancy.
Objective: To analyze variable peri-natal factors
that may be involved in the etiology of infantile
hypertrophic pyloric stenosis.
Methods: Over a two year's period, from January
2000 – December 2001, 31 cases of infantile
hypertrophic pyloric stenosis were evaluated for
variable peri-natal risk factors in AL-Eskan central
child teaching hospital for children.
Results: The 31 cases studied were 77.4% males
and 48.4% at three weeks of age. And of all cases,
51.6% were breast fed with a blood group (O) being
the predominant in 54.8%.
Normal vaginal delivery was in 80.6% of cases. All
infants 100% had vomiting, and 48.4% of them
presented with Jaundice and only 16.1% had
constipation. There were no significant correlations
between age and pyloric mass size, age and presence
of jaundice or between pyloric mass size and the
presence of jaundice.
Conclusion: Infantile hypertrophic pyloric stenosis
is a common condition affecting young infants and its
etiology remains unknown, more genetic and
environmental factors should be investigated in the
future.
Background: Geographic variations in the incidence of different congenital coronary anomalies are well known, but infrequently studied in the Iraqi population.
Recognition of coronary anomalies is important in patients undergoing coronary arteriogrphy; coronary interventions and cardiac surgery .Variation in the frequency of primary congenital coronary anomalies may possibly have a genetic background.
Patients and methods: Three thousands adult patients underwent diagnostic coronary angiography at two cardiac centers in Baghdad between January 2003 to March 2006. Their angiographic films were reviewed by at least two experts in coronary angiographic study.
Results: Among 3000 adult patients wh
Back ground: Congenital lobar Emphysema (CLE) is a rare yet serious condition which requires early detection and management, and usually present during infancy.
Patients and methods: This retrospective study aimed to review and evaluate methods adopted for the management of congenital lobar emphysema cases and it aimed to report and to document any observation which might need further research. The study retrospectively reviewed medical records of 53 cases whom were admitted to the department of thoracic surgery-medical city teaching complex over a period of 4 years (from June 2005 to June 2010). All of them had been diagnosed and managed as cases of congenital lobar emphysema based on their clin
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Summary:
Background: CM is the leading cause of infant deaths and account for much greater proportion of infant mortality’ than does premature birth. A malformation is a primary structural defect arising from a localized error in morphogenesis. This is a prospective study devoted to define the causes and frequencies of congenital malformations (CM) in Maternal and Children Hospital (MCH) in Al-Anbar govemorate (west of Iraq) and a comparison is done with other Iraqi and international studies.
FdC Med Baghdad Methods: Congenital malformations were studied over a period of 2 years from the 1st of July 2000 2007/ Vol. 49, No.3 f0 fjle 30th ofJune 2002 in 12831 births including stillbirths at MCH in Al- Anbar govemorate (west Receive
Background: Congenital pouch colon is an usual abnormality associated with anorectal malformation in which the colon is partially or totally replaced by a pouch like dilatation connected to the genitourinary tract by a fistula(colovesical).The condition varies from complete absence of normal colon with the ileum opening into colonic pouch to the presence of nearly normal colon with only the rectum or recto sigmoid being attached to a pouch which in turn connected to bladder by a band or fistula.
Objective: is to evaluate the methods of diagnosis and management of(C.P.C) with studying environmental factors especially pesticides and its prevalence.
Patients and Methods: A total number of seven cases of(C.P.C) associated with high typ
Background: Congenital anomaly is any alteration present at birth of normal anatomic structure and has cosmetic, medical or surgical significance
Objective: To determine the pattern of congenital anomalies in neonates admitted to tertiary neonatal care unit and to determine the impact of some factors related to congenital anomalies with and without congenital anomalies.
Patients and methods: A case control study was carried out during 6 months period (1St of January to 30th of June 2011). Neonates with and without congenital anomalies admitted to Children Welfare Teaching Hospital were included in the study as a case and control group. Demographic characteristics of both parents and neonates, Consangui
Background: Among individuals who have a stenotic aortic valve, a precise assessment of aortic valve area is essential for clinical judgment. So far, no studies have been conducted to investigate and assess the role of the three dimensional echo-cardiography in the assessment of the valve stenosis. This study aims to compare and assess the precision of the measurement of the stenosis area of the aortic valve by 2D versus 3D echo-cardiography.
(10)
Background: Congenital malformations are responsible for a considerable proportion of perinatal, neonatal and infant mortality in many Eastern Mediterranean countries. So this study
aims to find out the incidence, types and probable risk factors of these malformations in Baghdad.
Patients and methods: one hundred cases of congenital malformations were studied out of 8090 neonates born in 4 hospitals in Baghdad province over 5 months in 2002 (preterm, term) .The incidence , types and risk factors were analysed.
Results: the incidence of congenital malformations was 12.36/ 1000 live births, with the central nervous system malformations being the commonest. There is increased risk in consanguinous mar
(4)