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Risk factors and recurrence of fetal congenital anomalies

Thesis

Last updated: 06 Feb 2023

Subjects

-

Tags

Obstetrics & Gynecology

Advisors

Abdel-Raouf, Maged A. , Husain, Eiman A. , Abd-Manaf, Muhammad H.

Authors

El-Naggar, Muhammad Mansi Metwalli

Accessioned

2017-07-12 06:40:36

Available

2017-07-12 06:40:36

type

M.Sc. Thesis

Abstract

Congenital anomaly consists of a departure from normal anatomical architecture of organ or system. The prevalence of congenital anomalies detected at birth is about 2.5 % while long-term follow up studies increase the incidence to 14-15%. Congenital anomalies are the leading causes of infant mortality and one of the leading causes of long term morbidity. Causative factors of congenital malformations are divided into four major groups: single gene mutation, chromosomal abnormalities, multifactorial conditions and environmental factors. Birth defects can arise in at least three ways. The most common type of structural fetal abnormality is a malformation, an intrinsic abnormality "programmed" in development from the third to eight weeks, regardless of whether a precise genetic etiology is known. An example is spina bifida.

Issued

1 Jan 2012

DOI

http://dx.doi.org/10.21473/iknito-space/35632

Details

Type

Thesis

Created At

28 Jan 2023