Orphanet Journal of Rare Diseases (Mar 2021)

New insights in phenotype and treatment of lung disease immuno-deficiency and chromosome breakage syndrome (LICS)

  • Brigitte W. M. Willemse,
  • Saskia N. van der Crabben,
  • Wilhelmina S. Kerstjens-Frederikse,
  • Wim Timens,
  • Joris M. van Montfrans,
  • Caroline A. Lindemans,
  • Jaap Jan Boelens,
  • Marije P. Hennus,
  • Gijs van Haaften

DOI
https://doi.org/10.1186/s13023-021-01770-z
Journal volume & issue
Vol. 16, no. 1
pp. 1 – 7

Abstract

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Abstract We report five patients with lung disease immuno-deficiency and chromosome breakage syndrome (LICS) but without recurrent infections and severe immunodeficiency. One patient had extended survival to 6.5 years. Hematopoietic stem-cell transplantation failed to cure another patient. Our findings suggest that the immunological abnormalities can be limited and do not fully explain the LICS phenotype.

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