# Clinical evaluation of pediatric olfactory disorders: a review from etiology to management

**Authors:** Eleonora M. C. Trecca, Marella Reale, Luca Leone, Michele Cassano, Antonio della Volpe, Ignazio La Mantia, Fabio Pagella, Elena Cantone

PMC · DOI: 10.3389/falgy.2026.1741382 · Frontiers in Allergy · 2026-01-21

## TL;DR

This paper reviews how to diagnose and manage olfactory disorders in children, emphasizing the need for early detection and multidisciplinary care.

## Contribution

The paper proposes a structured clinical framework for evaluating and managing pediatric olfactory disorders.

## Key findings

- Olfactory disorders in children have diverse causes, including congenital syndromes and inflammatory conditions.
- Multidisciplinary collaboration is essential for accurate diagnosis and effective management of pediatric OD.
- Standardized age-specific diagnostic protocols and normative data remain limited in pediatric populations.

## Abstract

Olfactory perception plays a fundamental role in nutrition, emotional development, and social behavior, yet olfactory disorders (OD) in children remain largely underrecognized and understudied. This mini review summarizes current evidence and proposes a structured clinical approach for the evaluation and management of pediatric OD. Etiologies are diverse, encompassing congenital syndromes such as Kallmann and CHARGE, post-infectious and post-traumatic forms, inflammatory airway diseases, and structural or iatrogenic causes. Accurate diagnosis begins with a detailed medical history and comprehensive ENT examination, complemented by psychophysical olfactory testing adapted for pediatric populations. Although several validated tools exist—such as the Sniffin’ Sticks, U-Sniff, Pediatric Smell Wheel, and pBOT-6—standardized age-specific protocols and normative data remain limited. Imaging techniques, particularly MRI, provide valuable insights into congenital and acquired abnormalities of the olfactory bulbs and tracts, while CT is reserved for sinonasal or bony pathology. Multidisciplinary collaboration among pediatricians, neurologists, endocrinologists, geneticists, and otolaryngologists is essential to achieve etiological precision. Management strategies depend on the underlying cause and include medical or surgical treatment for reversible conditions, intranasal corticosteroids for inflammatory diseases, and olfactory training for post-infectious or congenital forms. Regular follow-up with objective testing and family education supports recovery and long-term adaptation. Despite the scarcity of pediatric-specific evidence, this review highlights the need for awareness, early diagnosis, and individualized management of OD in children, proposing a practical diagnostic and therapeutic framework to guide clinical decision-making in everyday ENT practice. A structured search strategy was applied to summarize the currently available evidence and highlight practical implications for clinical care.

## Linked entities

- **Diseases:** Kallmann syndrome (MONDO:0018800), CHARGE syndrome (MONDO:0008965)

## Full-text entities

- **Diseases:** OD (MESH:D000857), congenital syndromes (MESH:D008209), Kallmann (MESH:D017436), inflammatory airway diseases (MESH:D007249), CHARGE (MESH:D058747), congenital and acquired abnormalities of the olfactory (MESH:D000013)

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12868189/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12868189/full.md

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Source: https://tomesphere.com/paper/PMC12868189