Log in to save to my catalogue

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_proquest_miscellaneous_2852631203

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

Journal title

Clinical medicine insights. Case reports, 2023, Vol.16, p.11795476231193896-11795476231193896

Language

English

Formats

More information

Scope and Contents

Contents

BackgroundBardet-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 conge...

Alternative Titles

Full title

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

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_2852631203

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2852631203

Other Identifiers

ISSN

1179-5476

E-ISSN

1179-5476

DOI

10.1177/11795476231193896

How to access this item