Chromosomal abnormalities and copy number variations in fetal ventricular septal defects
نویسندگان
چکیده
منابع مشابه
Copy number variations in spermatogenic failure patients with chromosomal abnormalities and unexplained azoospermia.
Male infertility is mostly caused by spermatogenic failure. Currently, routine genetic analyses of unexplained azoospermia or oligozoospermia are limited to the investigation of Y chromosomal microdeletions and chromosome karyotype analyses. The aim of this study was to find spermatogenic failure genes in patients with chromosomal abnormalities and unexplained azoospermia caused by copy number ...
متن کاملAssociation of Fetal and Parental Chromosomal Abnormalities with Congenital Anomalies
Background & Aims: Chromosome abnormalities are a major cause of miscarriage and neonatal mortality. The present study aimed to determine the association of fetal and parents chromosomal abnormalities with congenital anomalies. Methods: A cross-sectional study was performed in a tertiary referral center (Afzalipour Hospital) over 16 months period (2011-2012). The study groups consisted of 77 fe...
متن کاملVentricular Septal Defects
An analysis was made of the 23 cases of isolated ventricular septal defects seen at autopsy over a 20year period at a children's hospital. All of the deaths occurred during the first 15 months of life. In addition to the clinical and morphologic findings, cardiac catheterization data obtained on 6 of the infants are presented. A wide range of electrocardiographic variation with respect to ventr...
متن کاملVentricular septal defects.
Ventricular septal defects are the most common congenital heart defect. They vary greatly in location, clinical presentation, associated lesions, and natural history. The present article describes the clinical aspects of ventricular septal defects and current management strategies.
متن کاملVentricular septal defects in adults.
Ventricular septal defects are one of the most common congenital cardiac malformations and can be associated with many types of congenital and acquired heart disease.
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ژورنال
عنوان ژورنال: Molecular Cytogenetics
سال: 2018
ISSN: 1755-8166
DOI: 10.1186/s13039-018-0408-y