Literature DB >> 422640

Orthopaedic problems in adult hypophosphatasia: a report of two cases.

J M Anderton.   

Abstract

Hypophosphatasia in adults is rare. Two elderly sisters presenting with pathological fractures of the femur are reported to illustrate the difficulties in orthopaedic management of this disease. All patients with a history of repeated fractures, especially from minor trauma and with generalised radiological bony abnormality, should be screened for this rare disease. A consistently low level of serum alkaline phosphatase with the presence of phosphoethanolamine in the urine is diagnostic.

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Year:  1979        PMID: 422640

Source DB:  PubMed          Journal:  J Bone Joint Surg Br        ISSN: 0301-620X


  4 in total

1.  Adult hypophosphatasia without apparent skeletal disease: "odontohypophosphatasia" in four heterozygote members of a family.

Authors:  F Eberle; S Hartenfels; H Pralle; A Käbisch
Journal:  Klin Wochenschr       Date:  1984-04-16

2.  Multiple fractures, pain, and severe disability in a patient with adult-onset hypophosphatasia.

Authors:  Neil A Braunstein
Journal:  Bone Rep       Date:  2015-10-30

3.  Burden of disease in pediatric patients with hypophosphatasia: results from the HPP Impact Patient Survey and the HPP Outcomes Study Telephone interview.

Authors:  Eric T Rush; Scott Moseley; Anna Petryk
Journal:  Orphanet J Rare Dis       Date:  2019-08-16       Impact factor: 4.123

4.  Bilateral Femoral Neck Fractures in A Young Patient Suffering from Hypophosphatasia, Due to A First Time Epileptic Seizure.

Authors:  N Sharma; E Bache; T Clare
Journal:  J Orthop Case Rep       Date:  2015 Jul-Sep
  4 in total

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