[Updating neonatal neurometabolic screening].
Israel Alfonso, Gustavo Charria
Abstract
Israel Alfonso, Gustavo Charria
Abstract
The purpose of neurometabolic screening is the earliest possible detection of treatable disorders. The disorders currently offered to general population screening are phenylketonuria, congenital hypothyroidism, galactosemia, congenital adrenal hyperplasia, cystic fibrosis, biotinidase deficiency, maple syrup urine disease, sickle cell disease, homocystinuria. The methods used for these evaluations are mass spectroscopy and genetic testing.
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The purpose of neurometabolic screening is the earliest possible detection of treatable disorders. The disorders currently offered to general population screening are phenylketonuria, congenital hypothyroidism, galactosemia, congenital adrenal hyperplasia, cystic fibrosis, biotinidase deficiency, maple syrup urine disease, sickle cell disease, homocystinuria. The methods used for these evaluations are mass spectroscopy and genetic testing.
Key concepts: Galactosemia, Maple syrup urine disease, Homocystinuria, Biotinidase deficiency, Medicine, Newborn screening, Congenital hypothyroidism, Cystic fibrosis