Haemoglobin O Arab in the Pomak population of Thrace. 1996

G Skaragas, and G Koliakos, and E Repanta, and K Zaphiriou, and A Chatziachmet, and A Dimitriadou, and N Papazoglou, and A Trakatellis
Internal Medicine Clinic, First General Hospital Agios Pavlos, Thessaloniki, Greece.

A 21 year old woman from Thrace with clinical and laboratory findings of mild hemolysis, was found to be homozygous for haemoglobin O Arab. Blood samples from 15 members of her family and from 42 inhabitants of her village were examined for the presence of Hb O Arab. A high incidence of this variant allele was also detected among the patient's family members as well as in other inhabitants of the village (p = 0.274 +/- 0.049). The possibility that Pomaks, a culturally unique tribe with controversial ethnic origin, may represent one of the original pools for the geographic distribution of the gene in the broader area of the Mediterranean basin is discussed.

UI MeSH Term Description Entries
D008297 Male Males
D010375 Pedigree The record of descent or ancestry, particularly of a particular condition or trait, indicating individual family members, their relationships, and their status with respect to the trait or condition. Family Tree,Genealogical Tree,Genealogic Tree,Genetic Identity,Identity, Genetic,Family Trees,Genealogic Trees,Genealogical Trees,Genetic Identities,Identities, Genetic,Tree, Family,Tree, Genealogic,Tree, Genealogical,Trees, Family,Trees, Genealogic,Trees, Genealogical
D005006 Ethnicity A group of people with a common cultural heritage that sets them apart from others in a variety of social relationships. Ethnic Groups,Nationality,Ethnic Group,Nationalities
D005260 Female Females
D006115 Greece A country in southern Europe, bordering the Aegean Sea, Ionian Sea, and the Mediterranean Sea, between Albania and Turkey. The capital is Athens. Crete,Macedonia (Greece)
D006444 Hemoglobin C A commonly occurring abnormal hemoglobin in which lysine replaces a glutamic acid residue at the sixth position of the beta chains. It results in reduced plasticity of erythrocytes.
D006451 Hemoglobin, Sickle An abnormal hemoglobin resulting from the substitution of valine for glutamic acid at position 6 of the beta chain of the globin moiety. The heterozygous state results in sickle cell trait, the homozygous in sickle cell anemia. Hemoglobin S,Deoxygenated Sickle Hemoglobin,Deoxyhemoglobin S,Hemoglobin SS,Hemoglobin, Deoxygenated Sickle,SS, Hemoglobin,Sickle Hemoglobin,Sickle Hemoglobin, Deoxygenated
D006455 Hemoglobins, Abnormal Hemoglobins characterized by structural alterations within the molecule. The alteration can be either absence, addition or substitution of one or more amino acids in the globin part of the molecule at selected positions in the polypeptide chains. Abnormal Hemoglobins
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults

Related Publications

G Skaragas, and G Koliakos, and E Repanta, and K Zaphiriou, and A Chatziachmet, and A Dimitriadou, and N Papazoglou, and A Trakatellis
January 1966, Nature,
G Skaragas, and G Koliakos, and E Repanta, and K Zaphiriou, and A Chatziachmet, and A Dimitriadou, and N Papazoglou, and A Trakatellis
January 1965, Nature,
G Skaragas, and G Koliakos, and E Repanta, and K Zaphiriou, and A Chatziachmet, and A Dimitriadou, and N Papazoglou, and A Trakatellis
April 1984, Journal of medical genetics,
G Skaragas, and G Koliakos, and E Repanta, and K Zaphiriou, and A Chatziachmet, and A Dimitriadou, and N Papazoglou, and A Trakatellis
October 1960, British medical journal,
G Skaragas, and G Koliakos, and E Repanta, and K Zaphiriou, and A Chatziachmet, and A Dimitriadou, and N Papazoglou, and A Trakatellis
January 1991, Clinical and laboratory haematology,
G Skaragas, and G Koliakos, and E Repanta, and K Zaphiriou, and A Chatziachmet, and A Dimitriadou, and N Papazoglou, and A Trakatellis
December 1999, British journal of haematology,
G Skaragas, and G Koliakos, and E Repanta, and K Zaphiriou, and A Chatziachmet, and A Dimitriadou, and N Papazoglou, and A Trakatellis
February 2005, Haematologica,
G Skaragas, and G Koliakos, and E Repanta, and K Zaphiriou, and A Chatziachmet, and A Dimitriadou, and N Papazoglou, and A Trakatellis
April 1976, Pathology,
G Skaragas, and G Koliakos, and E Repanta, and K Zaphiriou, and A Chatziachmet, and A Dimitriadou, and N Papazoglou, and A Trakatellis
August 2009, International journal of laboratory hematology,
G Skaragas, and G Koliakos, and E Repanta, and K Zaphiriou, and A Chatziachmet, and A Dimitriadou, and N Papazoglou, and A Trakatellis
February 1992, BMJ (Clinical research ed.),
Copied contents to your clipboard!