Extract Within the chILD-EU register, we are longitudinally following 221 individuals with persistent tachypnoea of infancy (PTI, also referred to as neuroendocrine cell hyperplasia of infancy (NEHI)) diagnosed by a multidisciplinary team specialised in childhood interstitial lung disease (chILD) 1. Since its description in 2022, SRRM2-haploinsufficiency has been associated with neurodevelopmental delay (NDD), obesity 2–6 and, in at least one case, the PTI/NEHI phenotype 3.
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Rapp et al. (Sun,) studied this question.
synapsesocial.com/papers/69a767e1badf0bb9e87e2bb5 — DOI: https://doi.org/10.1183/13993003.02135-2025
Christina Rapp
München Klinik
Julia Rodler
LMU Klinikum
Katharina Mauss-Schwarzer
German Center for Lung Research
European Respiratory Journal
University of Würzburg
Medical University of Graz
German Center for Lung Research
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