Microbiota–Metabolome Alterations Suggest Pro‐Inflammatory Phenotype in Congenital Central Hypoventilation Syndrome
Congenital central hypoventilation syndrome (CCHS) is a genetic disorder caused by mutations in the PHOX2B gene, characterized by impaired autonomic control of breathing and systemic consequences that may affect gut homeostasis. This study provides the first integrated multi‐omics analysis in a CCHS group and matched c...