Literature DB >> 21342251

Hypophosphatasia in a child with widened anterior fontanelle: lessons learned from late diagnosis and incorrect treatment.

Angelika Mohn1, Chiara De Leonibus, Tommaso de Giorgis, Etienne Mornet, Francesco Chiarelli.   

Abstract

UNLABELLED: Hypophosphatasia is characterized by deficiency of serum alkaline phosphatase with defective bone and teeth mineralization. We report on an 11-month-old boy who developed a complex clinical picture characterized by bulging anterior fontanelle, growth failure, nephrocalcinosis and impaired bone mineralization during high-dose calcium and vitamin D supplementation. This therapy had been started 5 months earlier for a presumed diagnosis of nutritional rickets established on the grounds of isolated widened anterior fontanelle. However, laboratory investigations revealed reduced alkaline phosphatase levels associated with hypercalcemia, hypercalciuria, low PTH and normal 25-hydroxy vitamin D levels. Genetic testing detected a compound heterozygote for the novel mutation (c.262G>A) and the described mutation (c.920C>T) in the ALPL gene.
CONCLUSION: High calcium and vitamin D supplementation should not be started in the presence of isolated signs of nutritional rickets without assessing calcium-phosphate metabolism. In fact, in rare bone-mineralizing disorders, this combined therapy might induce severe clinical complications.
© 2011 The Author(s)/Acta Paediatrica © 2011 Foundation Acta Paediatrica.

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Year:  2011        PMID: 21342251     DOI: 10.1111/j.1651-2227.2011.02228.x

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN: 0803-5253            Impact factor:   2.299


  7 in total

Review 1.  Hypophosphatasia: Biological and Clinical Aspects, Avenues for Therapy.

Authors:  Jean Pierre Salles
Journal:  Clin Biochem Rev       Date:  2020-02

Review 2.  Hypophosphatasia: From Diagnosis to Treatment.

Authors:  Sebastian Simon; Heinrich Resch; Klaus Klaushofer; Paul Roschger; Jochen Zwerina; Roland Kocijan
Journal:  Curr Rheumatol Rep       Date:  2018-09-10       Impact factor: 4.592

3.  Healthcare resource utilization in the management of hypophosphatasia in three patients displaying a spectrum of manifestations.

Authors:  Anjali B Daniel; Vrinda Saraff; Nick J Shaw; Robert Yates; M Zulf Mughal; Raja Padidela
Journal:  Orphanet J Rare Dis       Date:  2018-08-16       Impact factor: 4.123

4.  The Clinical Picture of Patients Suffering from Hypophosphatasia-A Rare Metabolic Disease of Many Faces.

Authors:  Izabela Michałus; Aneta Gawlik; Katarzyna Wieczorek-Szukała; Andrzej Lewiński
Journal:  Diagnostics (Basel)       Date:  2022-03-30

5.  Six ALPL gene variants in five children with hypophosphatasia.

Authors:  Na Su; Min Zhu; Xinran Cheng; Ke Xu; Roland Kocijan; Huijiao Zhang
Journal:  Ann Transl Med       Date:  2021-05

6.  A reference interval study for common biochemical analytes in Eastern Turkey: a comparison of a reference population with laboratory data mining.

Authors:  Ebubekir Bakan; Harun Polat; Yesim Ozarda; Nurinnisa Ozturk; Nurcan Kilic Baygutalp; Fatma Zuhal Umudum; Nuri Bakan
Journal:  Biochem Med (Zagreb)       Date:  2016       Impact factor: 2.313

7.  Could Alerting Physicians for Low Alkaline Phosphatase Levels Be Helpful in Early Diagnosis of Hypophosphatasia?

Authors:  Asma Deeb; Abubaker Elfatih
Journal:  J Clin Res Pediatr Endocrinol       Date:  2017-08-02
  7 in total

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