THE LACK OF ISOLATED PALATAL CLEFTS IN CZECH GYPSIES
Peterka M.1, 2, Peterková R.1, Likovský Z.1
1Department of Teratology, Institute of Experimental Medicine, Academy of Sciences of the Czech Republic, Prague, and 2Cleft Center, Clinic of Plastic Surgery, Faculty Hospital Královské Vinohrady, Prague, Czech Republic |
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Summary:
Orofacial clefts are usually divided into three basic types: isolated cleft lip (CL), cleft lip and palate (CLP) and isolated
cleft palate (CP). The incidence of specific cleft types in a population and their relative numbers show specific
differences between ethnic groups and races. However, there are no available data about the incidence and relative
numbers of orofacial cleft types (CL, CLP, CP) in the gypsy ethnic group. The aim of this study was to compare
relative numbers of specific types of orofacial clefts between the Czech gypsy and non-gypsy populations.We
conducted a retrospective epidemiological study using a set of all living patients with orofacial clefts born in the
Czech Republic from 1964 until 2002. The cleft patients were subdivided into three groups: 5304 non-gypsy children,
both parents of whom were non-gypsies (NN), 98 gypsy children, both parents of whom were gypsies (GG)
and 18 children with one parent non-gypsy and one parent gypsy (NG).
The relative number of isolated CP was 37.1% in NN children. However, the relative number of CP was significantly
reduced to 5.1% (P<0.01) in the GG group. Conversely, the relative number of CLP was higher (P<0.01) in the GG
group (62.2%) in comparison to the NN group (39.2%). The tendency to decrease in the relative number of CP and
increase in the relative number of CLP was also apparent in the NG group, but not so well expressed.We hypothesize
that the decrease in CP and increase in CLP and CL in gypsies might be caused by their genetic predisposition
to CL. Since the CP originates later than CL during embryonic development, some CP arise in embryos
with already existing CL giving rise to CLP. Consequently, the missing isolated CP might be hidden in the group of
CLP patients postnatally.
Key words:
orofacial clefts, epidemiology, birth defects, cleft palate, genetic predisposition
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