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Sensorineural Hearing Loss and Its Relationship with Duration of Chelation Among Major β-Thalassemia...

Sensorineural Hearing Loss and Its Relationship with Duration of Chelation Among Major β-Thalassemia...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6802818

Sensorineural Hearing Loss and Its Relationship with Duration of Chelation Among Major β-Thalassemia Patients

About this item

Full title

Sensorineural Hearing Loss and Its Relationship with Duration of Chelation Among Major β-Thalassemia Patients

Publisher

Palo Alto: Cureus Inc

Journal title

Curēus (Palo Alto, CA), 2019-08, Vol.11 (8), p.e5465-e5465

Language

English

Formats

Publication information

Publisher

Palo Alto: Cureus Inc

More information

Scope and Contents

Contents

IntroductionThalassemia is a common genetic disorder worldwide, also occurring frequently in Karachi, Pakistan. Beta (β)-thalassemia major patients need repeated transfusions which cause iron overload. Patients are treated with chelating agents to reduce the high serum ferritin level and to decrease morbidity and mortality due to increased iron lev...

Alternative Titles

Full title

Sensorineural Hearing Loss and Its Relationship with Duration of Chelation Among Major β-Thalassemia Patients

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6802818

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6802818

Other Identifiers

ISSN

2168-8184

E-ISSN

2168-8184

DOI

10.7759/cureus.5465

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