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Pediatric Genetic Diseases

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Division of Pediatric Genetic Diseases diagnoses the diseases that are secondary to genetic factors or develop due to genetic predisposition, such as hereditary diseases, genetic syndromes and congenital anomalies, starting at prenatal period.

Treatment and follow-up schedules are planned for these patients and also for families, if necessary; risks are analyzed and notified to parents in genetic counseling sessions. Prevention and screening programs are developed to protect individuals, families and general population against genetic diseases.

Update Date: 03 February 2020

Publish Date: 27 January 2020

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