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J Clin Pathol 2006;59:440-442 doi:10.1136/jcp.2005.026369
  • Short report

Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white family

  1. M F Campagnoli1,*,
  2. A Pucci2,*,
  3. E Garelli1,
  4. A Carando1,
  5. C Defilippi3,
  6. R Lala4,
  7. G Ingrosso5,
  8. I Dianzani6,
  9. M Forni2,
  10. U Ramenghi1
  1. 1Paediatric Department, University of Turin, Turin, Italy
  2. 2Division of Pathological Anatomy, Department of Clinical Pathology, Paediatric Hospital Regina Margherita, Turin
  3. 3Radiology Department, Paediatric Hospital Regina Margherita
  4. 4Endocrinology Unit, Paediatric Hospital Regina Margherita
  5. 5Orthopaedic Unit, Paediatric Hospital Regina Margherita
  6. 6Department of Medical Sciences, University of Eastern Piedmont, Novara, Italy
  1. Correspondence to:
    Professor Ugo Ramenghi
    Haematology Unit, Paediatric Department, University of Turin, Piazza Polonia 94, Torino 10126, Italy; ugo.ramenghi{at}unito.it
  • Accepted 9 May 2005

Abstract

Background: Familial tumoral calcinosis (FTC) is a rare autosomal recessive disease characterised by the development of multiple calcified masses in periarticular soft tissues; GALNT3 gene mutations have recently been described in an African American and in a Druse Arab family with FTC.

Objective: To report the clinical and histological features caused by a new GALNT3 mutation in a white family.

Results: Homozygosity for the nonsense mutation Lys463X was found in both affected siblings, who displayed a classic phenotype, the male also having testicular microlithiasis. He is the first subject described with testicular microlithiasis in FTC.

Conclusions: The high testicular expression of GALNT3 suggests that the gene alteration could act locally by causing deposition of calcium, and the testis may be an underestimated site of calcification in FTC. Autoimmune diseases are present in several members of the family. Although immune disorders have been described in FTC, autoimmunity does not segregate with the GALNT3 mutation in this family.

Footnotes

  • ↵* These authors contributed equally to the study

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