THU0618 Hypophosphatasia in french tertiary care hospitals
THU0618 Hypophosphatasia in french tertiary care hospitals
About this item
Full title
Author / Creator
Ebstein, E. , Thomas, T. , Cortet, B. , Briot, K. and Roux, C.
Publisher
Kidlington: Elsevier Limited
Journal title
Language
English
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Publication information
Publisher
Kidlington: Elsevier Limited
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Scope and Contents
Contents
BackgroundHypophosphatasia is a rare heritable metabolic disorder. Its prevalence is estimated at 1: 1 00 000. Its diagnosis can only be established after genetic confirmation. A low serum total alkaline phosphatase (ALP) level is the hallmark for the diagnosis of hypophosphatasia. Its prevalence is 0.05% in the general population and may be associ...
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Full title
THU0618 Hypophosphatasia in french tertiary care hospitals
Authors, Artists and Contributors
Author / Creator
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Record Identifier
TN_cdi_proquest_journals_2071216791
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2071216791
Other Identifiers
ISSN
0003-4967
E-ISSN
1468-2060
DOI
10.1136/annrheumdis-2018-eular.4491
