Genetic study of Welsh gypsies.
نویسندگان
چکیده
A South Wales gypsy kindred of Romany origin had a high incidence of phenylketonuria along with other recessively inherited disorders. There was a high degree of consanguinity (F = 0-017) with an excess of non-specific mental subnormality among known consanguineous matings. Phenylketonuria and a number of other recessively inherited disorders have been recorded from other Romany gypsy populations, but it is uncertain whether this results from a generally high gene frequency for the disorders or from consanguinity and other more local factors.
منابع مشابه
Genetic markers in Welsh gypsies.
Data are presented on polymorphic genetic markers of 84 Welsh gypsies, members of an inbred population characterised by a high incidence of phenylketonuria and other recessively inherited diseases. Sixteen polymorphic loci were studied: the ABO blood group distribution was comparable to that of the surrounding population, the B gene frequency being 7-5%, a lower frequency than most earlier stu...
متن کاملPERSONAL PRACTICE Health care needs of Travellers
Who are Travellers? The 1968 Caravan Sites Act ignored ethnicity and cultural distinctiveness by defining Travellers as: “persons of nomadic habit, whatever their race or origin”. However, in 1989, when the Commission for Racial Equality determined that Gypsies formed a distinct ethnic group, diVerences between “real Gypsies” and other more recent groups of Travellers were emphasised. There are...
متن کاملHealth care needs of Travellers
Who are Travellers? The 1968 Caravan Sites Act ignored ethnicity and cultural distinctiveness by defining Travellers as: “persons of nomadic habit, whatever their race or origin”. However, in 1989, when the Commission for Racial Equality determined that Gypsies formed a distinct ethnic group, diVerences between “real Gypsies” and other more recent groups of Travellers were emphasised. There are...
متن کاملA newly discovered founder population: the Roma/Gypsies.
The Gypsies (a misnomer, derived from an early legend about Egyptian origins) defy the conventional definition of a population: they have no nation-state, speak different languages, belong to many religions and comprise a mosaic of socially and culturally divergent groups separated by strict rules of endogamy. Referred to as "the invisible minority", the Gypsies have for centuries been ignored ...
متن کاملA common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from Spain.
Fanconi anemia (FA) is a genetic disease characterized by bone marrow failure and cancer predisposition. Here we have identified Spanish Gypsies as the ethnic group with the world's highest prevalence of FA (carrier frequency of 1/64-1/70). DNA sequencing of the FANCA gene in 8 unrelated Spanish Gypsy FA families after retroviral subtyping revealed a homozygous FANCA mutation (295C>T) leading t...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Journal of medical genetics
دوره 14 3 شماره
صفحات -
تاریخ انتشار 1977