congenital disorder

listen to the pronunciation of congenital disorder
الإنجليزية - التركية
(Tıp, İlaç) Doğuştan kusur/özür
الإنجليزية - الإنجليزية
(Tıp, İlaç) A physical defect present in a baby at birth that can involve many different parts of the body, including the brain, heart, lungs, liver, bones, and intestinal tract
{i} congenital defect, congenital abnormality, birth defect, defect present at birth
Structural abnormality (e.g., atresia, agenesis), functional problem (e.g., cystic fibrosis, phenylketonuria), or disease present at birth. Almost all are due to genetic factors (inherited or spontaneous mutations, chromosomal disorders), environmental influences during pregnancy (rubella or other maternal factors, exposure to toxins or radiation), or both. The most sensitive period is the first eight weeks after conception, during which time the human embryo is essentially formed. Major congenital malformations form during this period. Some inherited disorders result from simple Mendelian dominance or recessiveness. Others may involve multiple genes. Chromosomal disorders are rare, because few affected fetuses survive to be born. Environmental influences may affect only one of a pair of identical twins. At least 30 significant defects probably occur per 1000 births. See also birth defect; Down syndrome
congenital disorder

    الواصلة

    con·gen·i·tal dis·or·der

    التركية النطق

    kıncenıtıl dîsôrdır

    النطق

    /kənˈʤenətəl dəsˈôrdər/ /kənˈʤɛnətəl dɪsˈɔːrdɜr/
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