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

Liver Metabolomic Profiling Reveals Distinct Signatures Between Steatosis and Metabolic Dysfunction-Associated Steatohepatitis

Palomurto S, Flam E, Kaminska D, Virtanen KA, Kärjä V, Käkelä P, Pajukanta P, Eberlé D, Haas JT, Raverdy V, Caiazzo R, Pattou F, Staels[...]

Medications for Alcohol Use Disorder Among Patients With Severe Alcohol-Related Liver Disease

Sundaresh R, Singh J, Meza J, Saab S, Shetty A. Medications for Alcohol Use Disorder Among Patients With Severe Alcohol-Related Liver Disease. JAMA Netw Open.[...]

Quality of Gadoxetate-enhanced MRI versus US during Hepatocellular Carcinoma Screening in Participants with Cirrhosis

Lewis S, Wildman-Tobriner B, Cuevas J, Calle S, Bolger I, Wang K, Joshi H, Mankowski Gettle L, Yang JD, Min JH, Sirlin CB, Reeder SB,[...]