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Article

A comparison of sickle cell syndromes in northern Greece.

British journal of haematology - 1 Mar 1991

Christakis J, Vavatsi N, Hassapopoulou H, Angeloudi M, Papadopoulou M, Loukopoulos D, Morris J S, Serjeant B E, Serjeant G R

Abstract excerpt

Haematological and clinical characteristics have been examined in 30 patients with homozygous sickle cell (SS) disease, 28 with sickle cell-beta zero thalassaemia, and 21 with sickle cell-beta+ thalassaemia. The latter could be divided into three groups on their molecular basis and HbA levels, four subjects with an IVS-2 nt 745 mutation having 3-6% HbA (designated S beta+ thalassaemia type I), 14 subjects with an...

Topics

Adolescent
Adult
Anemia, Sickle Cell
Bone Diseases
Child
Child, Preschool
Female
Humans
Male
Middle Aged
Mutation
Splenomegaly

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Syndrome

Thalassemia

Source

Identifiers

PMID: 2012764
DOI: 10.1111/j.1365-2141.1991.tb08589.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-2012764-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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