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The aim of newborn screening is to detect diagnostic markers of treatable disorders in blood spots collected from presymptomatic newborns.
Early identification significantly improves long-term prognosis, minimizes complications, avoids unnecessary diagnostic testing, and helps families receive timely prenatal genetic counselling.
G6PD
TSH
Phenyl alanine
Cystic fibrosis
17-Hydroxy Progesterone
Galactosemia
Biotinidase
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Executive Health Check up
Diabetic Profile Tests
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