Literature DB >> 2706857

Tumoral calcinosis in two infants.

J L Rodriguez-Peralto1, F Lopez-Barea, A Torres, J I Rodriguez-Gonzalez, J Diaz-Faes.   

Abstract

Tumoral calcinosis (TC) is an uncommon disease, characterized by deposits of large, calcified painless soft-tissue masses around major joints in otherwise healthy children and young adults. This condition is a rare inherited metabolic disorder of unknown etiology. Biochemical findings are normal except for its occasional association with hyperphosphatemia. The youngest occurrence reported in the literature on TC may be one case of a five-month-old boy. The authors report here on two younger infants with TC, one aged ten days and the other aged three months, who were followed for more than three years and observed to completely recover all motorskeletal functions.

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Year:  1989        PMID: 2706857

Source DB:  PubMed          Journal:  Clin Orthop Relat Res        ISSN: 0009-921X            Impact factor:   4.176


  3 in total

1.  A rare disorder: tumoral calcinosis and cirrhosis.

Authors:  Seyyed Farshad Allameh; Akram Ghadiri Anari; Mehrnaz Asadi Gharabaghi; Manouchehr Nakhjavani
Journal:  BMJ Case Rep       Date:  2011-08-17

2.  Tumoral Calcinosis in Infancy. A light and electron microscopic study with X-ray microanalysis.

Authors:  Károly Balogh; Tamás Ferencz; András Csikós; József Tímár
Journal:  Pathol Oncol Res       Date:  1995       Impact factor: 3.201

Review 3.  Long-term clinical outcome and phenotypic variability in hyperphosphatemic familial tumoral calcinosis and hyperphosphatemic hyperostosis syndrome caused by a novel GALNT3 mutation; case report and review of the literature.

Authors:  Silje Rafaelsen; Stefan Johansson; Helge Ræder; Robert Bjerknes
Journal:  BMC Genet       Date:  2014-09-24       Impact factor: 2.797

  3 in total

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