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National Congenital Anomaly and Rare Disease Registration Service: patient leaflet

What NCARDRS does, the benefits of registering, and how we look after your information.

Documents

The National Congenital Anomaly and Rare Disease Registration Service: what it is, the benefits and your options

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Details

GPs and clinicians can use this leaflet when they speak to parents whose baby has a congenital anomaly or rare disease.

GPs and clinicians can contact the regional offices for printed copies of this leaflet.

Published 1 July 2015