Diagnosing a metabolic disorder in newborns - Dr. Chandra Kumar N of Cloudnine Hospitals
Автор: Doctors' Circle World's Largest Health Platform
Загружено: 2017-12-05
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Metabolic disorders can be diagnosed either by screening that is where we screen the newborn babies for these Metabolic diseases where we take blood sample from baby by heel prick and send it for analysis. So this is called as screening and you diagnose the disease before the baby becomes symptomatic, that is the baby develops symptoms due to this metabolic disease. The next group is where you diagnose the metabolic disorders where the baby has shown already the symptoms of metabolic disease. So the baby has developed lethargy or poor feeding, the baby becomes dull, the baby may throw some seizures, the baby becomes unresponsive. In such a baby, you suspect metabolic disease and you send the sample for screening. So in such babies also you can diagnose metabolic disease. So you can diagnose metabolic disease by screening actively for metabolic disease before the baby becomes symptomatic or after the baby develops the disease, then also you can diagnose the metabolic disease.
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