DIAGNOSTICS OF INHERITED DISEASES AND CONGENITAL DEVELOPMENT LESIONS IN NEWBORNS
Abstract
Genetic screening of hemoglobinopathies, G6 PD anzyme deficiency, phenylketonuria
and hypothyreosis in newborns was carried out by means of modern techniques. Congenital
development lesions as hydrocephalia, unencephalia, Spina bifida, hypospadia, cryptarchism,
skeletal abnormalities were shown. Gen and phenotypic frequencies were calculated
for the identified diseases
and hypothyreosis in newborns was carried out by means of modern techniques. Congenital
development lesions as hydrocephalia, unencephalia, Spina bifida, hypospadia, cryptarchism,
skeletal abnormalities were shown. Gen and phenotypic frequencies were calculated
for the identified diseases
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