PURPOSE Kabuki syndrome is a multiple congenital malformation syndrome, with characteristic facial features, mental retardation, and skeletal and congenital heart anomalies. However, the cardiac anomalies are not well described in the Korean population. We analyzed the cardiac anomalies and clinical features of Kabuki syndrome in a single tertiary center. METHODS A retrospective analysis was ...

Background: Mullerian duct malformations delineate a group of congenital anomalies that result from arrested development, or incomplete fusion of the mesonephric ducts. In many patients, uterine anomalies have been related with infertility, recurrent pregnancy loss, prematurity and other obstetric complications which increase perinatal morbidity and mortality rates, where as in others these mal...

BACKGROUND Adversities operating over intrauterine life have been associated with risk of schizophrenia, but the biology of resultant developmental perturbation is poorly understood. AIMS To examine the relationship of congenital anomalies and related functional impairments in infancy to risk of schizophrenia. METHOD Using the Congenital Anomalies data-set from the Prenatal Determinants of ...

Address for Correspondence: Dr. V. Sailaja, MD (Anatomy), Assistant Professor, Department of Anatomy, Kamineni Institute of Medical Sciences, Nalgonda, Telangana, India. E-Mail: [email protected] Aims and Objectives: Assess the association of the congenital malformations with maternal age & analyse the congenital malformations, involving various systems of the body system wise. Materials and...

Congenital anomalies of the kidney and ureter are a significant cause of morbidity in foetus, neonate, infancy and adulthood. Radiological investigations provide a foundation for diagnosing these conditions giving vital clinical information. Various imaging modalities used to diagnose these anomalies are intravenous urography (IVU), voiding cystourethrogram (VCUG), Computed tomography (CT), Mag...

Congenital hairy polyps are exceedingly rare congenital anomalies. We report a case of congenital hairy polyp arising from posterior tonsillar pillar which was excised with bipolar cautry.