Expanded newborn screening: Guiding principles, concerns and relevance

Since its introduction in 1960s, universal newborn screening (NBS) using the heel-prick dried blood spot samples has become an integral part of public health system in developed countries expanded to pre-symptomatic detection of specific inherited metabolic, endocrine and hematologic disorders. In o...

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Päätekijät: Seema Pavaman Sindgikar (Tekijä), Rathika Damodar Shenoy (Tekijä)
Aineistotyyppi: Kirja
Julkaistu: Wolters Kluwer Medknow Publications, 2014-01-01T00:00:00Z.
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Yhteenveto:Since its introduction in 1960s, universal newborn screening (NBS) using the heel-prick dried blood spot samples has become an integral part of public health system in developed countries expanded to pre-symptomatic detection of specific inherited metabolic, endocrine and hematologic disorders. In our country, NBS may become relevant with epidemiological shift and increasing access to technology. Current recommendations include a phased introduction of screening for congenital hypothyroidism, congenital adrenal hyperplasia and glucose 6-phosphate dehydrogenase deficiency. In this review, the guiding principles of NBS, some of the individual disorders, the concerns and relevance to our country are discussed. Establishing a pre- and post-screening care and education are of utmost priority before NBS is adapted into health care system.
Huomautukset:0975-9727
10.4103/0975-9727.128951