'Klippel-Fiel Syndrome\r'

'Klippelâ€Feil syndrome is a precise rare disease. It was reported for the first clipping in 1912 by Maurice Klippel and Andre Feil. It has been characterized by the amalgamation of any 2 of the 7 cervical vertebrae. The syndrome occurs in a heterogeneous collection of patients unified only by the heading of a defect in the organisation or segmentation of the spine. Klippelâ€Feil syndrome can be identified by shortness of the fill in. Those with the syndrome comport a very low hairline and the talent of the neck to move is limited or none.Some symptoms acknowledge: ?Scoliosis, which is a case-to-side bow of the spine, which is abnormal. The spine sometimes appears as a â€Å"C” or an â€Å"S”. ?Spina bifida is when the spinal canal and the back bone do not close completely during birth. ? tornado Palate, which is a hole in the crownwork of the mouth ?Respiratory problems ?Heart malformations ? piteous stature The actual prevalence of Klippel-Feil synd rome is mystical due to the fact that there was no study done to determine the aline prevalence.Although the actual occurrence for the KFS syndrome is unknown, it is estimated to occur 1 in 42,000 newborns worldwide. In addition, females seem to be affected slightly more practically than males Treatment for Klippelâ€Feil syndrome is symptomatic and may include cognitive process to relieve cervical or craniocervical instability and constriction of the spinal cord, and to clear up scoliosis. The heterogeneity of this syndrome has made it difficult to blueprint the diagnosis as well as the prognosis classes for this disease.Because of this, it has complicated the exact exposition of the genetic etiology of the syndrome. The prognosis for intimately individuals is good if the disorder is treated too soon on and appropriately. Activities that can injure the neck should be avoided, as it may alter to further damage. Other diseases associated with the syndrome can be fatal if not treated, or if piece too late to be treatable. Although, surgery is an option it’s not highly recommended.My sister suffers from this disorder; therefore I see it every day. Surgery was given to my mother as an option precisely there were far worse side effects to the aftermath of the surgery than reasonable living with the disorder for the rest of her life. She didn’t choose to claim surgery because any it would have paralyzed her or could have possibly killed her. The disorder has affected her by not allowing her to use her neck at all, which makes it very difficult for her to do the things that we can.\r\n'