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All you need to know aboutPANCREATIC EXOCRINE INSUFFICIENCY (PEI)Our Digestive System The Digestive System runs from the mouth to the anus and includes the stomach, the large and small bowels (intestines)

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How to fill out congenital and inherited anomalies

01

Obtain a detailed family history to identify any inherited anomalies

02

Consult with a genetic counselor to determine the risk of passing on genetic anomalies

03

Conduct diagnostic tests such as genetic testing or ultrasound imaging to detect congenital anomalies in a fetus

04

Monitor the pregnancy closely for any signs of anomalies and follow any recommended treatment plans

05

Keep accurate medical records and communicate with healthcare providers about any concerns or findings related to congenital and inherited anomalies

Who needs congenital and inherited anomalies?

01

Individuals who have a family history of genetic disorders or birth defects

02

Pregnant women who want to assess the risk of passing on genetic anomalies to their children

03

Parents of children with known congenital anomalies who require ongoing medical care and support

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What is congenital and inherited anomalies?

Congenital anomalies are conditions present at birth that are either inherited or caused by environmental factors affecting fetal development.

Who is required to file congenital and inherited anomalies?

Healthcare providers, hospitals, and laboratories are required to file reports on congenital and inherited anomalies.

How to fill out congenital and inherited anomalies?

Healthcare providers must fill out a standardized reporting form with detailed information about the anomaly and the affected individual.

What is the purpose of congenital and inherited anomalies?

The purpose of reporting congenital and inherited anomalies is to track and monitor the prevalence of these conditions for public health surveillance and research purposes.

What information must be reported on congenital and inherited anomalies?

Information such as the type of anomaly, date of birth, genetic history, and relevant medical history must be reported on congenital and inherited anomalies.

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