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[Molecular identification of Hemoglobin D Punjab in cases detected in two families].

Revista medica del Instituto Mexicano del Seguro Social - 1 Jan 2000

Bouchán-Valencia Patricia, Coeto-Barona Georgina, Rosenfeld-Mann Fany, Trueba-Gómez Rocío, Baptista-González Héctor, Rivera-Echegoyén Mariano, Rodríguez-Terán Gerardo, Martínez-Villegas Octavio

Abstract excerpt

BACKGROUND: Hemoglobin D Punjab is the world most common variant hemoglobin D; in Mexico there are reports of isolated cases. Our goal is to present the clinical and molecular study in two families with HbD Punjab. The objective was to submit molecular diagnosis of two families with Hb D Punjab and clinical features. CLINICAL CASE: Family 1: neonate with maternal history of HbS carrier. Father and sister with...

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PMID: 27819792

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HFE

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

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Related research

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Research trail→

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[Molecular identification of Hemoglobin D Punjab in cases detected in two families].PMID 27819792Read ↗

Hemoglobin D-Punjab: origin, distribution and laboratory diagnosisSemantic proximity Read ↗

[The association of beta zero-thalassemia and Hb D Punjab in a family of Indian origin. The second case reported in Spain].Semantic proximity Read ↗

Molecular characterization of hemoglobin D Punjab traits and clinical-hematological profile of the patients.Semantic proximity Read ↗

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Clinical and hematological presentation among Indian patients with common hemoglobin variants.Semantic proximity Read ↗

Missing Hb Q-India Peak in a Triple-Heterozygous Patient with Hb D-Punjab/Hb Q-India/β-Thalassemia Trait.Semantic proximity Read ↗

Coexistence of rare variant HbD Punjab [α2β2(121(Glu→Gln))] and alpha 3.7 kb deletion in a young boy of Hindu family in West Bengal, India.Semantic proximity Read ↗

Co-inheritance of Hb D-Punjab (codon 121; GAA-->CAA) and beta (0) -thalassemia (IVS-II-1;G-->A).Semantic proximity Read ↗

Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis.Semantic proximity Read ↗

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β-globin gene haplotypes linked with the Hb D-Punjab [β121(GH4)Glu→Gln, GAA>CAA] mutation in eastern India.Semantic proximity Read ↗

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