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Information to help healthcare professionals speak with parents, following suspected or confirmed diagnosis of congenital heart disease.
NCARDRS records those people with congenital abnormalities and rare diseases across the whole of England.
Data by National Congenital Anomaly and Rare Disease Registration Service (NCARDRS) showing estimates of birth prevalence of congenital anomalies in England.
This template is used to notify GPs of a suspected positive newborn blood spot screening result of congenital hypothyroidism (CHT).
Information for parents about congenital hypothyroidism (CHT) following a baby’s screening test result.
This leaflet can help healthcare professionals speak with people, following suspected or confirmed diagnosis of congenital diaphragmatic hernia (CDH).
The report is based on registration data collected by National Congenital Anomaly and Rare Disease Registration Service (NCARDRS) in NDRS (Data Services Directorate).
Guidance on the referral and management of babies with congenital hypothyroidism (CHT).
This statistical release describes congenital anomalies in babies born or delivered in 2021.
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