Targeted questionnaires improve detection of early gastrointestinal symptoms in young children with Fabry disease

Targeted questionnaires elicit early gastrointestinal symptoms in pediatric Fabry disease patients that would otherwise go unnoticed at a standard doctor's appointment. Based on manual analysis of questionnaire data, a list of questions is suggested to support pediatricians of young patients with FD in recognizing GI symptoms. Use of more targeted and specific questions regarding GI symptoms is warranted in pediatric appointments of patients with FD, with age-appropriate expansion of the questions at 24 months of age. Early detection of symptoms in this population is critical as individual treatment plans are based on symptom onset and as newborn screening is expanding.

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Publication Details

Journal
Orphanet Journal of Rare Diseases
Published
2026-01-20
DOI
https://doi.org/10.1186/s13023-025-04168-3
Primary Topic
Lysosomal Storage Disorders Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Targeted questionnaires improve detection of early gastrointestinal symptoms in young children with Fabry disease

Gwen Gunn, Niwa Ali, Hannah Waddel, Jared J. Druss et al.
Orphanet Journal of Rare Diseases
Lysosomal Storage Disorders Research
article

Targeted questionnaires improve detection of early gastrointestinal symptoms in young children with Fabry disease

Gwen Gunn, Niwa Ali, Hannah Waddel, Jared J. Druss, Anika L. Quillin, Dawn Laney, William Wilcox
article en

Abstract

Targeted questionnaires elicit early gastrointestinal symptoms in pediatric Fabry disease patients that would otherwise go unnoticed at a standard doctor's appointment. Based on manual analysis of questionnaire data, a list of questions is suggested to support pediatricians of young patients with FD in recognizing GI symptoms. Use of more targeted and specific questions regarding GI symptoms is warranted in pediatric appointments of patients with FD, with age-appropriate expansion of the questions at 24 months of age. Early detection of symptoms in this population is critical as individual treatment plans are based on symptom onset and as newborn screening is expanding.

Orphanet Journal of Rare DiseasesVol. 21(1)
Emory University (US)
Sanofi, Emory University, Amicus Therapeutics, Sanofi Genzyme
Good health and well-being
Openalex Percentile: Top 84%
Lysosomal Storage Disorders Research
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