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Title: CATCH 22 Syndrome. Author: Yonehara Y, Nakatsuka T, Ichioka S, Sasaki N, Kobayashi T. Journal: J Craniofac Surg; 2002 Sep; 13(5):623-6. PubMed ID: 12218787. Abstract: CATCH 22 syndrome is characterized by cardiac defects, abnormal facial features, thymic hypoplasia, cleft palate, and hypocalcemia. It results from a deletion within chromosome 22q11. This syndrome is not a simple disease. It includes DiGeorge syndrome, conotruncal anomaly face syndrome, and velocardiofacial syndrome. The authors report two cases of CATCH 22 syndrome.[Abstract] [Full Text] [Related] [New Search]