Interstitial lung disease in children: ultra-rare genetic variants from national registry of Türkiye - Amsterdam 2025

New insights into paediatric rare lung and airway disease

Chair(s): Anna Wiemers, Jing Yuan

Session type: Poster session

Interstitial lung disease in children: ultra-rare genetic variants from national registry of Türkiye

Sati Özkan Tabakçi

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Interstitial lung disease in children: ultra-rare genetic variants from national registry of Türkiye

Sati Özkan Tabakçi

Poster

Abstract

Quality of Life in Turkish Children with Interstitial Lung Disease: Insights from the National ChILD Registry

Handan Kekec

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Primary ciliary dyskinesia: analysis of symptoms at diagnosis according to genetic defect

Laura Petrarca

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Understanding Pulmonary Fibrosis in Pediatric Interstitial Lung Disease:A Comprehensive Analysis

Handan Kekec

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Clinical Profile and Outcomes of Children with chemical pneumonitis after Hydrocarbon Aspiration: A case series from a Tertiary Care Hospital in Western India

Jagdish Prasad Goyal

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Bridge Bronchus and Beyond: Unraveling the Complexity of Pediatric Bronchovascular Malformations

Adelina Procopi

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Chest computed tomography use in patients with Primary Ciliary Dyskinesia

Nicola Ullmann

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A decade of primary ciliary dyskinesia diagnosis in children: insights from a Portuguese tertiary hospital

Isabel Moitinho De Almeida

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Exploring epithelial dysfunction in primary ciliary dyskinesia

Elizabeth Haughey

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Variability in the interpretation of Radiological Changes in Fibrosing Lung Disease in Childhood Interstitial Lung Disease

Elias Seidl

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Genotype-phenotype differences at the time of diagnosis in school-aged children with primary ciliary dyskinesia: an international central European multicentric study

Tereza Holecek Kristofová

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Interstitial lung disease in children with inborn errors of immunity: a systematic review

Heidi Schaballie

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Dental Health and Quality of Life in Children with Primary Ciliary Dyskinesia

Ezgi Kazanci Oztuna

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Clinical and imaging presentation in children with surfactant protein C gene mutation, a CRC chILD study

Celine Delestrain

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Clinical impact of age at diagnosis in pediatric primary ciliary dyskinesia

Nilgun Kula

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Lung malformation requiring double surgical excision in a patient with Niemann-Pick Disease

Mirko Gambino

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Sleep Disorders, Quality of Life, and Anxiety Levels of Caregivers in Children with Primary Ciliary Dyskinesia

Ayse Tana Aslan

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Childhood interstitial lung disease in metabolic disorders: prevalence, genotypic and clinical characteristics, and management approaches an analysis of the chILD-Turkey registry

Merve Selçuk Balci

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Genetic and Clinical Heterogeneity of Childhood Interstitial Lung Diseases: A Single-Center Experience

Ayyüce Ünlü

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CDN Connection Issue

The ERS Congress 2025, Amsterdam

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