Spina Bifida is a genetic disease
Introduction – overview of Spina Bifida
Spina bifida is Latin for 'split spine '. It is one of a class of serious birth defects called nerve-related tube defects (NTD). It is a something that’s different from what’s usually expected of the folding of the rear end away from the head surface of the embryo, which usually forms the spine related column with its muscles and the spinal cord and the spinal nerves. It is known as one of the most complex diseases scientific research believes that is caused by the interaction of multiple genetic and environmental factors. But very few factors have been identified, but many still remain unknown. Individuals with spina bifida have changes in dozens of genes and their
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Before some babies at born they can be diagnosed with spina bifida, but the baby can undergo surgery when it is in it mother’s womb and this can repair or minimize the spinal detect. But the operation done by fetal surgeons may have an extensive risk assessment of mother and fetus. Another option is that you can treat the disease after the baby is born treatment may include ongoing surgery, medications and physical and behavioral therapy but could depended on the severity of the detect. People with the mildest form of spina bifida or spina bifida occulta they usually don’t need treatment. Myelomeningocele spina bifida is the most servere form of spina bifida, people with this type require surgery to prevent infections, further injury and also to correct he spinal defect. Babies with myelomeningocele majority of these babies develop hydrocephalus and that require treatment because they may develop a progressive tethering of the spina cord, this means that spine and vertebrae don’t stretch and you will just grow normally. But this may loss of muscle function in the legs, bladder and bowel. Surgery on the may be under conduct to restore full