Literature DB >> 6673484

Inherited isolated hyperphosphatasemia.

K Kruse.   

Abstract

An 11-year-old girl presented with permanent elevation of serum alkaline phosphatase activity (AP) exceeding 4 times the upper normal limit. Family investigations revealed a persistent increment of AP activity in the father and one of the two sisters, indicating a dominant form of inheritance. Physical examination and laboratory results were normal; isoenzyme studies revealed that the raised serum AP activity was mainly due to an increase of the bone isoenzyme. No disturbance of calcium or phosphate metabolism or morphological alterations of the skeleton could be demonstrated. This indicates an inherited abnormality in the metabolism of bone AP in the absence of disease.

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Year:  1983        PMID: 6673484     DOI: 10.1111/j.1651-2227.1983.tb09825.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN: 0001-656X


  4 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

2.  Evidence for infectious origin of isolated transient hyperphosphatasemia.

Authors:  U Frank; K Kruse
Journal:  Eur J Pediatr       Date:  1985-03       Impact factor: 3.183

3.  If Hoofbeats are not From Horses, It Could be Zebras!! Isolated Hyper-alkaline Phosphatasemia.

Authors:  Mahak Chauhan; David H Alpers; James P Hamilton; Paul J Thuluvath
Journal:  J Clin Exp Hepatol       Date:  2020-12-17

Review 4.  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

  4 in total

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