INTRODUCTION  
                           Spina bifida is a failure in the closure of the
                            vertebrae at the base of the neural tube resulting
                            in the herniation or exposure of the spinal cord
                            and/or meninges. The incidence of spina bifida is
                            similar to that of anencephalus. As with other neural
                            tube defects there are reported associations with
                            maternal insulin dependent diabetes, hyperthermia,
                            obesity at conception, autosomal trisomies, and low
                            serum folate concentrations. 
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                           ANTENATAL  
                           In the West Midlands programmes for the prenatal
                            diagnosis of neural tube defects are based on maternal
                            serum AFP screening performed at 16 to 20 weeks gestation
                            and ultrasound screening, which is widely performed
                            at 16 to 22 weeks for this purpose. AFP serum screening
                            is thought to be 80% sensitive for open spina bifida.
                            Ultrasound is based on examination of the fetal head,
                            particularly the shape of the skull and the appearance
                            of the cerebellum. Spina bifida is most often diagnosed
                            using the cranial signs of an abnormal shape of the
                            fetal skull (lemon shape) and flattening and loss
                            of the median sulcus in the cerebellum (banana shape).
                            Hydrocephalus is often associated with spina bifida
                            and the spine itself can be examined to demonstrate
                            failure of closure of the vertebral arches, lack
                            of skin cover and herniation. 
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                           POSTNATAL  
                           The prognosis for cases of spina bifida is not
                            necessarily fatal and depends on the location, size,
                            and extent of the defect, and the presence of hydrocephalus.
                            Cases with high extensive lesions with obvious hydrocephalus
                            at birth and other congenital defects are universally
                            poor. In surviving infants, spina bifida can result
                            in severe disability affecting the sensory and motor
                            function of the lower limbs, bowel, and bladder.
                            Predicting the outcome of open spina bifida cases
                            is problematic, with some cases having a good outcome,
                            while others have severe disability. The options
                            are either early surgical closure, with or without
                            shunting of hydrocephalus or waiting for a time to
                            allow the lesion to heal by granulation. 
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                           WEST
                                MIDLANDS DATA  
                           To be added. 
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