Expanding the Gastrointestinal Phenotype of 10p15.3 Microdeletion Syndrome: Refractory Atypical Gastroparesis in an Adult

By sjmartinez • February 18, 2025

Li J, Bachu V, Shahrvini B, Baniqued M, Haghighat S, Mallepally NR. Expanding the Gastrointestinal Phenotype of 10p15.3 Microdeletion Syndrome: Refractory Atypical Gastroparesis in an Adult. Cureus. 2025 Jan 16;17(1):e77555. doi: 10.7759/cureus.77555. PMID: 39958070; PMCID: PMC11829799.

Tags: 10p15.3 microdeletion syndrome, atypical gastroparesis, DGSOM Student, Digestive Diseases, dip2c gene, enteric nervous system dysfunction, gastroesophageal reflux disease, gastrointestinal motility disorders, General Internal Medicine, gerd, Olive View DoM, prucalopride, Publications, rare genetic disorders, refractory gastrointestinal disease, Resident, zmynd11 gene

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