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Neonatal Genetic Disorders
Neonatal genetic disorders refer to conditions resulting from variations or abnormalities in an infant's DNA. The manifestation of these disorders varies, with some causing metabolic challenges, developmental delays, or physical differences.
Early detection plays a pivotal role in managing these conditions. Some of these disorders might be identified during pregnancy through prenatal screenings, while others become evident after birth. Diagnosing these disorders involves a detailed physical examination, a comprehensive review of family medical history, and specific genetic tests. Once a genetic disorder is diagnosed, a team of experts, including healthcare providers and genetic counsellors, collaborates to devise a tailored management plan.
This plan aims to ensure the child experiences optimal growth and development. It might include specific treatments, therapies, and other support services, always keeping the child's best interests at heart and providing the family with the necessary guidance and support.
Consult our neonatal doctors if you need services related to Neonatal Genetics in Bangalore.
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