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

Disease-modifying influences of coexistent G6PD-deficiency, Gilbert syndrome and deletional alpha thalassemia in hereditary spherocytosis: A report of three cases.

Clinica chimica acta; international journal of clinical chemistry - 1 Jul 2016

Jamwal Manu, Aggarwal Anu, Kumar Verinder, Sharma Prashant, Sachdeva Man Updesh Singh, Bansal Deepak, Malhotra Pankaj, Das Reena

Abstract excerpt

BACKGROUND: Hereditary spherocytosis (HS) is a common inherited hemolytic anemia characterized by heterogeneous clinical presentations with variable degrees of anemia, jaundice, splenomegaly and gallstones. Although the underlying genetic defects in red cell membrane proteins may explain many phenotypic variations, a proportion of variability may be due to other co-inherited factors like enzymopathies,...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to alpha-Thalassemia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gilbert Disease

Share to Glucosephosphate Dehydrogenase Deficiency

Share to Mutation

Share to Neonatal Health and Biochemistry

Share to Sequence Deletion

Share to Spherocytosis, Hereditary

Source

Identifiers

PMID: 27108201
DOI: 10.1016/j.cca.2016.04.020

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Disease-modifying influences of coexistent G6PD-deficiency, Gilbert syndrome and deletional alpha thalassemia in hereditary spherocytosis: A report of three cases.PMID 27108201Read ↗

Hematological and molecular analysis of patients with G6PD deficiency revealed coexistent hereditary spherocytosis and alpha thalassemia.Semantic proximity Read ↗

Hematological parameters and red blood cell morphological abnormality of Glucose-6-Phosphate dehydrogenase deficiency co-inherited with thalassemiaSemantic proximity Read ↗

Glucose-6-phosphate dehydrogenase deficiencySemantic proximity Read ↗

A Case of hereditary spherocytosis coexisting with Gilbert's syndrome.Semantic proximity Read ↗

[Glucose-6-phosphate dehydrogenase deficiency and hereditary hemolytic anemia].Semantic proximity Read ↗

Rasburicase-induced hemolytic anemia in previously undiagnosed G6PD deficiency.Semantic proximity Read ↗

A Novel SPTA1 Mutation in a Patient with Hereditary Spherocytosis without a Family History and Coexisting Gilbert's Syndrome.Semantic proximity Read ↗

Chronic non-spherocytic haemolytic disorders associated with glucose-6-phosphate dehydrogenase variants.Semantic proximity Read ↗

[Glucose 6-phosphate dehydrogenase deficiency: a protection against malaria and a risk for hemolytic accidents].Semantic proximity Read ↗

Glucose-6-phosphate dehydrogenase deficiency in India.Semantic proximity Read ↗

Hemolytic anemias due to erythrocyte enzyme deficiencies.Semantic proximity Read ↗

Unusual Gilbert's syndrome genotype in a Greek patient suffering from both Gilbert's syndrome and familial mediterranean fever. A case report.Semantic proximity Read ↗

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