In this paper, the theme of medical neutrality is highlighted, in particular, definition concept and principles are defined, examples violation through prism armed aggression Ukraine given. Medical seen as a social agreement that obliges society to protect health workers both time war peacetime, personnel provide care all, regardless religion, race, ethnic origin, political affiliation or other...

BACKGROUND Ethnic disparities in perinatal mortality are well known. This study aimed to explore the contribution of demographic, socioeconomic, health behavioural and pre-existent medical risk factors among different ethnic groups on fetal and early neonatal mortality. METHODS We assessed perinatal mortality from 24.0 weeks' gestation onwards in 554 234 singleton pregnancies of nullip...

Ethnic identity is understood as a dynamic state, that is determined by three components: (1) by the degree of inclusion in the group of one's cultural origin; (2) the tendency to assimilate to the ethnic group of origin; and (3) the complementary tendency to differentiate from one's own ethnic group. In the same degree as the inclusion intensifies, the tendency to assimilate decreases and the ...

OBJECTIVE To examine the possible effects of discrimination by sex and race on the career patterns of doctors up to six years after qualifying. DESIGN Postal questionnaire follow up survey. PARTICIPANTS 1572 Doctors who graduated from five British medical schools in 1981, 1983, and 1985, including 587 women and 131 doctors from ethnic minorities. MAIN OUTCOME MEASURES Reported success rat...

Inborn errors of metabolism (IEM) are a heterogeneous group of genetic disorders present in all ethnic groups. We investigated the frequency of consanguinity among parents of newborns with IEM diagnosed by neonatal screening. Data were obtained from 15 years of expanded newborn screening for selected IEM with autosomal recessive mode of inheritance, a national screening program of newborns cove...

Citrin deficiency is an autosomal recessive disorder caused by mutation in the SLC25AJ3 gene. It has two major phenotypes: adult-onset type II citrullinemia (CTLN2) and neonatal intrahepatic cholestatic caused by citrin deficiency (NICCD). NICCD is characterized by neonatal/infantile-onset cholestatic hepatitis syndrome associated with multiple amino acidemia and hypergalactosemia. NICCD is sel...