与白人相比,斯洛伐克东部吉普赛人先天性甲状腺功能减退症的发病率增加。

Endocrinologia experimentalis Pub Date : 1989-06-01
M Lescisinová, M Kúseková, J Sedlák, V Murková, P Langer, O Pavkovceková
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引用次数: 0

摘要

吉普赛人占东斯洛伐克总人口的9%。然而,在对先天性甲状腺功能减退症(CH)进行强制性筛查的头三年半期间,有15,346名吉普赛新生儿,占90,760名新生儿总数的16.8%。其中吉卜赛新生儿有7例CH(即1∶2192),而在75,414例白人新生儿中有12例CH(即1∶6284),明显少于吉卜赛新生儿(P < 0.05)。由于在居住在斯洛伐克的吉普赛人新生儿中发现了迄今为止报道的任何欧洲人口或种族群体的最高近交系数(通过家谱法获得的Fg = 0.017,通过同姓法获得的Fi = 0.084),因此可能表明吉普赛人新生儿中CH的高发病率可能是由于某些遗传和遗传因素。虽然从目前的数据还不能明确地建立直接的相互关系,而且还远未阐明,但目前的观察可能被认为是对这一问题研究的贡献。
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Increased incidence of congenital hypothyroidism in Gypsies in east Slovakia as compared with white population.

Ethnic Gypsies represent 9 percent of total population of East Slovakia. However, during first three and half years of compulsory screening of congenital hypothyroidism (CH) there were 15,346 Gypsy newborns which was 16.8 percent of a total number of 90,760 newborns. Out of these Gypsy newborns 7 cases of CH were found (i.e. 1:2192), while 12 cases of CH were observed among 75,414 white newborns (i.e. 1:6284), which was significantly less than that in newborns Gypsies (P less than 0.05). Since the far highest coefficient of inbreeding ever reported for any European population or ethnic groups has been found by others in newborns Gypsies living in Slovakia (Fg = 0.017 obtained by genealogic method and Fi = 0.084 obtained by the method of isonymy), it may be suggested that a high incidence of CH in newborns Gypsies may be due to some genetic and hereditary factors. Though a direct interrelationship cannot be definitely established from the present data and still remains far from to be elucidated, the present observation may be considered as a contribution to the study of this problem.

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