OBJECTIVE Firstly, to assess the completeness of ascertainment in the National Congenital Anomaly System (NCAS), the basis for congenital anomaly surveillance in England and Wales, and its variation by defect, geographical area, and socioeconomic deprivation. Secondly, to assess the impact of the lack of data on pregnancies terminated because of fetal anomaly. DESIGN Comparison of the NCAS wi...

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 by an...

INTRODUCTION Aqueductal stenosis may be caused by a number of etiologies including congenital stenosis, tumor, inflammation, and, very rarely, vascular malformation. However, aqueductal stenosis caused by a developmental venous anomaly presenting as congenital hydrocephalus is even more rare, and, to the best of our knowledge, has not yet been reported in the literature. In this study, we revie...

INTRODUCTION Hypospadias is a congenital abnormality of the penis, in which there is incomplete development of the distal urethra. There are numerous reports showing na increase of prevalence of hypospadias. Association of craniofacial malformations in patients diagnosed with hypospadias is rare. The aim of this study is to describe the association between hypospadias and craniofacial congenita...

In 1976, Gonzales-Crussi et al. (Am. J. Dis. Child. 130:1015-18, 1976) introduced the first case of bridging bronchus as a rare bronchial branching anomaly; since then, only 14 worldwide cases was described. We suggest our case might be number 15 and could be the first case of type six of this bronchial anomaly. We present a case of a 10-month-old infant with bridging bronchus, congenital trach...

Retrocaval ureter also referred to as pre-ureteral vena cava is a rare congenital anomaly with the ureter passing posterior to the inferior vena cava. Though it is a congenital anomaly, patients do not normally present with symptoms until the 3rd and 4th decades of life from a resulting hydronephrosis. We present the first two cases to be reported in Ghana; a 36-year-old male and a 40-year-old ...

background: routine use of assisted hatching (ah) following icsi is a controversial issue in the literature. there are rare studies regarding the effect of laser assisted hatching (lah) on live birth rate. objective: our main goal was to evaluate the effect of lah on delivery rate as well as congenital anomaly in patients undergoing their first icsi cycle. materials and methods: a total of 182 ...

STUDY DESIGN Retrospective case study by clinical and radiological data analysis. PURPOSE To analyze different types of vertebral anomalies and the incidence of associated intraspinal anomalies in the Indian population. OVERVIEW OF LITERATURE This is the largest study of congenital scoliosis and associated intraspinal anomalies in Indian population. Incidence of intraspinal anomaly in this ...

BACKGROUND There is a strong maternal parent-of-origin effect in determining susceptibility to multiple sclerosis (MS). One hypothesis is that an abnormal intrauterine milieu leading to impaired fetal development could plausibly also result in increased susceptibility to MS. A possible marker for this intrauterine insult is the presence of a non-fatal congenital anomaly. METHODS We investigat...