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Genetics is a branch of medicine that focuses on the diagnosis and management of hereditary disorders. Human genetics is a field of scientific research that may or may not apply to medicine, and medical genetics refers to the application of genetics to medical care. Research on the causes and inheritance of genetic disorders can be considered within both human genetics and medical genetics, while the diagnosis, management, and counselling people with genetic disorders can be considered as part of medical genetics. Narayana Health is among the top genetics hospitals in India. The department of medical genetics offers state-of-the-art evaluation, diagnosis and treatment of various genetic disorders. Our multi-disciplinary team of doctors specialize genetics, syndrome identification, metabolic diseases and birth defects. They work in tandem with specialists from other departments to provide patients the most comprehensive care. We offer clinical genetics and related laboratory services. Clinical genetics pays attention to hereditary disorders, birth defects, developmental delay, epilepsy and so forth. Experts also treat patients with chromosomal rearrangements, Down syndrome, Fragile X syndrome, Neurofibromatosis, Turner syndrome and Williams syndrome. Our lab can conduct tests that help in identifying and evaluating the size, shape and number of chromosomes; this helps in detecting missing chromosomes.
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