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Early diagnosis of ataxia telangiectasia in the neonatal phase: a parents' perspective
- Source :
- European Journal of Pediatrics, 179, 2, pp. 251-256, European Journal of Pediatrics. SPRINGER, European Journal of Pediatrics, European Journal of Pediatrics, 179, 251-256
- Publication Year :
- 2019
- Publisher :
- SPRINGER, 2019.
-
Abstract
- Ataxia telangiectasia (A-T) is a severe neurodegenerative disorder with variable immunodeficiency. Together with the Dutch A-T community, we investigated the opinion of A-T parents on an early A-T diagnosis in the asymptomatic phase of the disease. During an annual national meeting for A-T patients and families, the topic of an early A-T diagnosis was discussed in relation to the recent introduction of neonatal screening for severe combined immunodeficiency (SCID) in the Netherlands. Based on the discussion, individual arguments were identified and processed into a questionnaire, which was sent out to 64 A-T parents (32 families). Arguments included were insecurity to diagnosis, possible medical advantages, appropriate genetic counseling and family planning, loss of “golden” year(s), and early cancer screening for parents. The response rate was 55% (n = 35 parents). Twenty-six (74%) parents felt that the advantages of an early diagnosis outweighed the disadvantages, five parents thought that the disadvantages would outweigh the advantages (14%), and four parents did not indicate a preference. Conclusion: The majority of parents of a child with A-T would have preferred an early diagnosis during the asymptomatic phase of the disease, because the uncertainty during the diagnostic process had had a major impact on their lives. In addition, the knowledge of being carriers of an ATM gene mutation influenced decisions about family planning. Parents who opposed against an early diagnosis emphasized the joy of having a seemingly healthy child until diagnosis.What is Known:• Ataxia telangiectasia (A-T) is a devastating DNA repair disorder with a huge impact on quality of life of patients and their parents.• Patients with A-T may incidentally be identified at birth as the consequence of neonatal screening for severe combined immunodeficiency (SCID).What is New:• The majority of Dutch parents of A-T patients (74%) would have preferred an early diagnosis of their child in the asymptomatic phase of the disease.• Major arguments for an early A-T diagnosis were (1) the experienced insecurity in diagnostic trajectories and its impact on families and (2) the knowledge of being ATM mutation carriers when deciding about family planning. An argument against an early diagnosis is losing the joy of having a seemingly healthy child until diagnosis.
- Subjects :
- Adult
Male
Parents
0301 basic medicine
Pediatrics
medicine.medical_specialty
Genetic counseling
lnfectious Diseases and Global Health Radboud Institute for Molecular Life Sciences [Radboudumc 4]
Genetic Counseling
Disease
Risk Assessment
Asymptomatic
Parents perspective
03 medical and health sciences
Neonatal Screening
0302 clinical medicine
Quality of life
Surveys and Questionnaires
medicine
Humans
Genetic Predisposition to Disease
Parent-Child Relations
Immunodeficiency
Netherlands
Response rate (survey)
Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7]
business.industry
Incidence
Infant, Newborn
Metabolic Disorders Radboud Institute for Molecular Life Sciences [Radboudumc 6]
Middle Aged
medicine.disease
Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3]
Early diagnosis
3. Good health
030104 developmental biology
Family planning
Child, Preschool
Parents opinion
Pediatrics, Perinatology and Child Health
Ataxia-telangiectasia
Ataxia telangiectasia
Female
Original Article
medicine.symptom
business
030217 neurology & neurosurgery
Subjects
Details
- Language :
- English
- ISSN :
- 03406199
- Database :
- OpenAIRE
- Journal :
- European Journal of Pediatrics, 179, 2, pp. 251-256, European Journal of Pediatrics. SPRINGER, European Journal of Pediatrics, European Journal of Pediatrics, 179, 251-256
- Accession number :
- edsair.doi.dedup.....b782308821cdd08a107a613b4f561b21