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|February 28, 2021 at 8:34 PM EST - Updated February 28 at 8:34 PM CHARLESTON, S.C. (WCSC) - Sunday marked National Rare Disease Day to raise awareness for thousands of unique and uncommon conditions. At just two weeks old, Abby Cate Zaucha’s symptoms began baffling both her parents and doctors. “It presented with symptoms like acid reflux or milk protein allergies,” Mother Melissa Zaucha said. After thousands of dollars and months of trial and error, she was diagnosed with Congenital Sucrase-Isomaltase Deficiency, or CSID, which makes it impossible to break down certain sugars and starches. The disease only affects 0.2 percent of North Americans.

United statesMelissa zauchaNational rare disease dayNational human genome instituteAbby cate zauchaCongenital sucrase isomaltase deficiencyNational human genomeஒன்றுபட்டது மாநிலங்களில்தேசிய ரேர் நோய் நாள்தேசிய மனிதன் மரபணு நிறுவனம்தேசிய மனிதன் மரபணு