Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Student screening for inherited blood disorders in Bahrain.

Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit - 1 May 2003

Al-Arrayed S, Hafadh N, Amin S, Al-Mukhareq H, Sanad H

Abstract excerpt

In Bahrain and neighbouring countries inherited disorders of haemoglobin, i.e. sickle-cell disease, thalassaemias and glucose-6-phosphate dehydrogenase (G6PD) deficiency, are common. As part of the National Student Screening Project to determine the prevalence of genetic blood disorders and raise awareness among young Bahrainis, we screened 11th-grade students from 38 schools (5685 students), organized lectures...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Glucosephosphate Dehydrogenase Deficiency
Share to Health Education

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Health Services Needs and Demand

Share to Hemoglobin E

Share to Hemoglobinopathies

Share to Hemoglobins, Abnormal

Share to Sickle Cell Trait

Share to Thalassemia

Source

Identifiers

PMID: 15751927

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Student screening for inherited blood disorders in Bahrain.PMID 15751927Read ↗

Knowledge, Attitude, and Practice Regarding Premarital Genotype Counselling and Testing for Sickle Cell Disease Among the Academic Staff of Kaduna State University, NigeriaSemantic proximity Read ↗

Prevalence of Hemoglobinopathies (β-Thalassemia and Sickle Cell Trait) in the Adult Population of Al Majma'ah, Saudi Arabia.Semantic proximity Read ↗

Pre-marital screening for sickle cell haemoglobin and genetic counseling: awareness and acceptability among undergraduate students of a Nigerian UniversitySemantic proximity Read ↗

Knowledge of Sickle cell Anemia, Attitude and perception towards Premarital genotype counseling and screening among Youths of Dala LGA Kano, Nigeria.Semantic proximity Read ↗

Outcome of premarital genetic counseling for couples at risk of hemoglobinopathies in Kingdom of BahrainSemantic proximity Read ↗

Review of the spectrum of genetic diseases in Bahrain.Semantic proximity Read ↗

Knowledge and Attitude Toward the Hemoglobinopathies Premarital Screening Program in Saudi Arabia: Population-Based SurveySemantic proximity Read ↗

Marked regional variations in the prevalence of sickle cell disease and β-thalassemia in Saudi Arabia: findings from the premarital screening and genetic counseling program.Semantic proximity Read ↗

Distribution of haemoglobin genotypes, knowledge, attitude and practices towards sickle cell disease among unmarried youths in the Buea Health District, Cameroon.Semantic proximity Read ↗

Frequency of haemoglobinopathies at premarital health screening in Dohuk, Iraq: implications for a regional prevention programmeSemantic proximity Read ↗

Screening for thalassemia and other hemoglobinopathies in a tertiary care hospital of West Bengal: implications for population screening.Semantic proximity Read ↗

Frequency of haemoglobinopathies and glucose-6-phosphate dehydrogenase deficiency in BasraSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.