Cartilage-hair hypoplasia: follow-up of immunodeficiency in two patients

J Clin Immunol. 2014 Feb;34(2):256-9. doi: 10.1007/s10875-013-9981-3. Epub 2014 Jan 9.

Abstract

Purpose: To study the changes in the immunological status in 2 children with cartilage hair hypoplasia (CHH).

Methods: A 4-6 year immunological follow-up from infancy.

Results: In infancy the children presented a combined T cell and B cell immunodeficiency which partly resolved in time. Mitogen-induced T cell proliferation values fluctuated but lymphopenia has remained constant. Both patients had no recent thymic emigrants (TREC). Both children have suffered from a prolonged viral infection. Hypogammaglobulinemia normalized during the first years of life but both children have a specific antibody deficiency (SAD).

Conclusions: The changes in the immunological status in CHH patients emphasize the importance of a regular follow-up. SAD should be searched for in CHH. The absence of TRECs supports combined immunodeficiency and possible need of hematopoietic stem cell transplantation.

Publication types

  • Case Reports

MeSH terms

  • Female
  • Follow-Up Studies
  • Genotype
  • Hair / abnormalities*
  • Hair / immunology
  • Hirschsprung Disease / diagnosis
  • Hirschsprung Disease / genetics
  • Hirschsprung Disease / immunology*
  • Hirschsprung Disease / therapy
  • Humans
  • Immunity, Cellular / genetics
  • Immunity, Cellular / immunology
  • Immunity, Humoral / genetics
  • Immunity, Humoral / immunology
  • Immunologic Deficiency Syndromes / diagnosis
  • Immunologic Deficiency Syndromes / genetics
  • Immunologic Deficiency Syndromes / immunology*
  • Immunologic Deficiency Syndromes / therapy
  • Infant
  • Infant, Newborn
  • Lymphocyte Activation / immunology
  • Male
  • Mutation
  • Osteochondrodysplasias / congenital*
  • Osteochondrodysplasias / diagnosis
  • Osteochondrodysplasias / genetics
  • Osteochondrodysplasias / immunology
  • Osteochondrodysplasias / therapy
  • Primary Immunodeficiency Diseases

Supplementary concepts

  • Cartilage-hair hypoplasia