The Lifelong Impact of X-Linked Hypophosphatemia: Results From a Burden of Disease Survey
The Lifelong Impact of X-Linked Hypophosphatemia: Results From a Burden of Disease Survey
About this item
Full title
Author / Creator
Publisher
Washington, DC: Endocrine Society
Journal title
Language
English
Formats
Publication information
Publisher
Washington, DC: Endocrine Society
Subjects
More information
Scope and Contents
Contents
Abstract
Context
X-linked hypophosphatemia (XLH) is characterized by excess fibroblast growth factor 23 (FGF23), hypophosphatemia, skeletal abnormalities, and growth impairment. We aimed to understand the burden of disease of XLH across the lifespan.
Methods
Responses were collected from adults with XLH and parents/caregivers of a child...
Alternative Titles
Full title
The Lifelong Impact of X-Linked Hypophosphatemia: Results From a Burden of Disease Survey
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6595532
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6595532
Other Identifiers
ISSN
2472-1972
E-ISSN
2472-1972
DOI
10.1210/js.2018-00365
