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The report is based on registration data collected by National Congenital Anomaly and Rare Disease Registration Service (NCARDRS) in NDRS (Data Services Directorate).
These documents describe conditions screened for by the NHS fetal anomaly screening programme (FASP), including diagnostic tests and treatment options.
This template is used to notify GPs of a suspected positive newborn blood spot screening result of congenital hypothyroidism (CHT).
Guidance for specialists for initiation of valproate in female patients and for annual review and pregnancy testing to support adherence to pregnancy prevention requirements during the pandemic.
Public Health England's vision for a single National Congenital Anomaly and Rare Disease Registration Service (NCARDRS).
Prevalence (numbers and rates) of congenital anomalies in Wales 1998-2014 by condition, health board and unitary authority.
You do not need to tell DVLA if you have Chiari malformation.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Information for parents about congenital hypothyroidism (CHT) following a baby’s screening test result.
Advice for medical professionals to follow when assessing drivers with neurological disorders.
Information on the reporting, investigation and management of acute flaccid paralysis (AFP) and acute flaccid myelitis (AFM).
How to spot glanders and farcy, what to do if you suspect them and measures to prevent their spread.
An Integrated Screening Outcomes Surveillance Service (ISOSS) report on congenital syphilis in babies born after 1 January 2015 and reported by 30 June 2020.
Toxoplasmosis is an infection caused by Toxoplasma gondii (T. gondii) that can pass from mammals to humans.
Guidance on the referral and management of babies with congenital hypothyroidism (CHT).
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