Services

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• Expanded panel on Newborn Screening including dried blood spot analysis of nTSH assay for Congenital hypothyroidism; n17OHP for Congenital Adrenal Hyperplasia; nG6PD assay for Glucose-6-Phosphate Dehydrogenase Deficiency –www.nsisd.ruh.ac.lk
• Whole Exome Sequencing database of congenital hypothyroidism – Sri LankaDatabase of 50 children with CH are deposited in the archives of the Nuclear Medicine Unit. IF anyone seeks access drop an email to headnmu@med.ruh.ac.lk