Down Syndrome Disorder Discussion

Down Syndrome Disorder Discussion ORDER NOW FOR CUSTOMIZED AND ORIGINAL ESSAY PAPERS ON Down Syndrome Disorder Discussion Trisomy 21 Trisomy 21, by another name Down syndrome, has become the most common condition involving a chromosomal abnormality in the United States. The genetic disorder is usually characterized by intellectual disability, physical growth delays, and characteristic facial features. Diagnosing, treating and managing the condition is imperative for better development of individual Diagnosis Down Syndrome Disorder Discussion Down syndrome is detectable during pregnancy by administering prenatal tests. The condition can be diagnosed after birth through the use of Karyotype, a chromosomal analysis procedure. Newborn who have Trisomy 21 will require cardiology evaluation and echocardiography. Diagnostic and prenatal techniques have become more enhanced and are readily available. Fluorescent in situ hybridization in situ confirms the diagnosis, followed by chromosomal Karyotyping after birth. Children are supposed to have annual screening to check for hearing and vision (Allyse et al., 2017). Medication For Trisomy 21, drug therapy is currently not a standard form of care for the disease. There is no cure for Trisomy 21, but varieties of therapies and treatments addressing unique conditions for the disease exist. Occupational therapy, physical therapy, behavioral therapy, and speech therapy are used to positively impact the development of a child suffering from Trisomy 21. Surgical treatment can be done for cardiac anomalies among children suffering from the disease. Diuretics and digitalis should be given for cardiac management. Hypothyroidism should be checked and treated to prevent further intellectual deterioration. Management And Referral Assessment of child development should be done regularly to check the impacts of the disease and the growth of a child. Frequent consultation and adequate nutrition will be recommended. Referrals to the Don Syndrome team will be made where necessary if the medical needs arise and the condition gets serious. Annual review for the condition is fully recommended (Stewart, Gallagher & Leyden, 2018). Trisomy 21 needs to be checked as early as possible. To minimize the negative impacts of the disease, therapies and specific treatments for the unique condition that are brought by the disease need to be targeted. Management of the disease will require follow-up activities and consultation. References Allyse, M., Aypar, U., Bonhomme, N., Darilek, S., Dougherty, M., Farrell, R., … & Otto, L. (2017). Offering prenatal screening in the age of genomic medicine: A practical guide. Journal of Women’s Health, 26(7), 755-761. Stewart, R., Gallagher, D., & Leyden, P. (2018). Diagnosis and management of conductive hearing loss in children with trisomy 21. Journal of Paediatrics and Child Health, 54(11), 1242-1245. Get a 10 % discount on an order above $ 100 Use the following coupon code : NURSING10