Search results for "Nigerians"

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Odontogenic tumours in Nigeria : a multicentre study of 582 cases and review of the literature

2018

Background The objective of this study was to classify the various types of odontogenic tumours (OTs) using the newly updated 2017 world health organization (WHO) histological typing and to analyze the prevalence of these tumours among Nigerians as well as to compare the results obtained with reports from world-wide studies. Material and Methods The records of four major tertiary hospitals in Nigeria were reviewed over a 12-year (2004-2015) period. Lesions diagnosed as odontogenic tumours were classified into four groups according to the 2017 WHO histological typing. Data which consisted of age, sex and site were analyzed using SPSS for Window (version 20.0; SPSS Inc., Chicago, IL) and freq…

AdultMalemedicine.medical_specialtyAdolescentNigeriaOdontogenic TumorsReviewOdontogenic myxomaYoung Adult03 medical and health sciences0302 clinical medicineOdontomaPrevalencemedicineHumansYoung adultChildAmeloblastomaGeneral DentistryAgedRetrospective StudiesAdenomatoid odontogenic tumorbusiness.industryNigeriansRetrospective cohort study030206 dentistryMiddle Agedmedicine.disease:CIENCIAS MÉDICAS [UNESCO]DermatologyOdontogenicOtorhinolaryngology030220 oncology & carcinogenesisUNESCO::CIENCIAS MÉDICASFemaleSurgeryOral Surgerybusiness
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c.451dupT in KLKB1 is common in Nigerians, confirming a higher prevalence of severe prekallikrein deficiency in Africans compared to Europeans

2020

Essentials Prekallikrein (PK) deficiency is a recessive trait with isolated aPTT prolongation. KLKB1 c.451dupT is common in Nigerians (7/600 alleles) and absent in a European group (0/600). To date, all genotyped PK-deficient patients of African ancestry were homozygous for 451dupT. Diagnostics of isolated aPTT prolongation in African descendants should include PK testing. ABSTRACT: Background Severe prekallikrein deficiency (PK deficiency) is an autosomal-recessive condition thought to be very rare. Recently we reported that the previously unnoticed variant c.451dupT, p.Ser151Phefs*34 in KLKB1, which is listed in databases aggregating genome data, causes PK deficiency and is common in Afri…

medicine.medical_specialtyPopulationNigeria030204 cardiovascular system & hematology03 medical and health sciences0302 clinical medicineInternal medicineEpidemiologyPrevalenceHumansMedicineAlleleeducationAllele frequencyBlood coagulation testeducation.field_of_studymedicine.diagnostic_testbusiness.industryNigeriansPrekallikreinPrekallikreinHematologyBlood Coagulation DisordersKallikreinsbusinessPartial thromboplastin timeJournal of Thrombosis and Haemostasis
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