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This confidential report collects vital information on congenital anomalies for statistical purposes, safeguarding public health, and compliance with the Data Protection Act.
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It is a formal document used to report cases of congenital anomalies observed in newborns or infants to relevant public health authorities.
Healthcare providers such as hospitals, clinics, and physicians who diagnose or treat infants with congenital anomalies are typically required to file this report.
The report should be filled out by providing accurate patient information, details about the diagnosed anomalies, and any relevant clinical findings, ensuring compliance with confidentiality guidelines.
The purpose is to collect data on congenital anomalies for public health surveillance, research, and to improve healthcare services and outcomes for affected individuals.
Information typically includes the patient's demographics, specific details of the congenital anomaly, date of diagnosis, and any interventions provided.
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