1887

oa Current Allergy & Clinical Immunology - Living with X-linked agammaglobulinemia (XLA) in a developing country setting : clinical and counselling considerations in an affected family : primary immunodeficiency disorders

Volume 28, Issue 1
  • ISSN : 1609-3607

 

Abstract

X-linked agammaglobulinemia (XLA) is the prototype of humoral primary immunodeficiency disorders. Although the prognosis has improved in recent years, the outcome still varies in different social settings. We describe the clinical burden of XLA, the impact of living with it, and the role of genetic counselling for a family managed at Tygerberg Hospital.


Data was collected from clinical case notes and through semi-structured qualitative interviews with family members. A detailed pedigree of the family was used to highlight important clinical and genetic counselling considerations.
Factors that may result in the poor outcome in some members of this family included low socio-economic status and higher exposure to infection, delayed diagnosis, lack of adherence to intravenous immunoglobulin prophylaxis in adolescence and adulthood, irregular follow-up at the Clinical Immunology Service, and poor understanding of the condition. The high burden of disease and early death of affected individuals resulted in fear of the condition, and difficulties in communicating and adjusting to the diagnosis.
Primary immunodeficiency disorders, such as XLA, have a dramatic impact on the lives of affected individuals and families in a developing world setting. Genetic counselling has an important role to play in the comprehensive management of these families.

Loading full text...

Full text loading...

Loading

Article metrics loading...

/content/caci/28/1/EJC168678
2015-03-01
2019-12-10

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error