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Megaloblastic Anemia in Bardet-Biedl Syndrome: A Rare Case Report

Megaloblastic Anemia in Bardet-Biedl Syndrome: A Rare Case Report

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_59d7dd338459452f972702a9f79e6029

Megaloblastic Anemia in Bardet-Biedl Syndrome: A Rare Case Report

About this item

Full title

Megaloblastic Anemia in Bardet-Biedl Syndrome: A Rare Case Report

Publisher

London, England: SAGE Publications

Journal title

Clinical medicine insights. Case reports, 2023-01, Vol.16

Language

English

Formats

Publication information

Publisher

London, England: SAGE Publications

Subjects

Subjects and topics

More information

Scope and Contents

Contents

Background:
Bardet-Biedl syndrome (BBS) also known as Laurence-Moon-Bardet-Biedl syndrome one of the rarely reported genetic disorder characterized by an intellectual disability, limb, kidney abnormalities, obesity, and Rod-cone dystrophy. Other associated condition includes diabetes mellitus, hypertension, hypogonadism, facial dysmorphism, and...

Alternative Titles

Full title

Megaloblastic Anemia in Bardet-Biedl Syndrome: A Rare Case Report

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_59d7dd338459452f972702a9f79e6029

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_59d7dd338459452f972702a9f79e6029

Other Identifiers

ISSN

1179-5476

E-ISSN

1179-5476

DOI

10.1177/11795476231193896

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