Literature DB >> 3589775

Persistent isolated hyperphosphatasemia.

J M Lewis.   

Abstract

We have presented the case of a 7-year-old girl with a two-year history of elevated levels of serum alkaline phosphatase, without evidence of bone or liver disease. Family investigations showed minimal increases in SAP levels in both of her parents. Eight other families with persistent isolated hyperphosphatasemia have been reported previously. This disorder differs from transient isolated hyperphosphatasemia by its later age of detection (usually greater than 5 years), duration of elevation (greater than 1 year), elevation of bone isoenzyme levels alone, and frequent familial incidence.

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Year:  1987        PMID: 3589775     DOI: 10.1097/00007611-198706000-00032

Source DB:  PubMed          Journal:  South Med J        ISSN: 0038-4348            Impact factor:   0.954


  2 in total

1.  Familial increased serum intestinal alkaline phosphatase: a new variant associated with Gilbert's syndrome.

Authors:  A G Lieverse; G G van Essen; G J Beukeveld; J Gazendam; E C Dompeling; L P ten Kate; S A van Belle; J Weits
Journal:  J Clin Pathol       Date:  1990-02       Impact factor: 3.411

Review 2.  Benign familial hyperphosphatasaemia as a cause of unexplained increase in plasma alkaline phosphatase activity.

Authors:  S B Rosalki; A Y Foo; J S Dooley
Journal:  J Clin Pathol       Date:  1993-08       Impact factor: 3.411

  2 in total

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