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Frequency and age at occurrence of clinical manifestations of disease in patients with hypophosphata...

Frequency and age at occurrence of clinical manifestations of disease in patients with hypophosphata...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_38ed8f016f2d457597f90ee51492ec7a

Frequency and age at occurrence of clinical manifestations of disease in patients with hypophosphatasia: a systematic literature review

About this item

Full title

Frequency and age at occurrence of clinical manifestations of disease in patients with hypophosphatasia: a systematic literature review

Publisher

England: BioMed Central Ltd

Journal title

Orphanet journal of rare diseases, 2019-04, Vol.14 (1), p.85-85, Article 85

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

Hypophosphatasia (HPP) is a rare, inherited, metabolic disease caused by tissue-nonspecific alkaline phosphatase deficiency, characterized by bone mineralization defects and systemic complications. Understanding of the clinical course and burden of HPP is limited by its rarity. This systematic literature review and synthesis of case report data aim...

Alternative Titles

Full title

Frequency and age at occurrence of clinical manifestations of disease in patients with hypophosphatasia: a systematic literature review

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_38ed8f016f2d457597f90ee51492ec7a

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_38ed8f016f2d457597f90ee51492ec7a

Other Identifiers

ISSN

1750-1172

E-ISSN

1750-1172

DOI

10.1186/s13023-019-1062-0

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