Wilson D I, Burn J, Scambler P, Goodship J
Division of Human Genetics, University of Newcastle upon Tyne, UK.
J Med Genet. 1993 Oct;30(10):852-6. doi: 10.1136/jmg.30.10.852.
DiGeorge syndrome (DGS) comprises thymic hypoplasia, hypocalcaemia, outflow tract defects of the heart, and dysmorphic facies. It results in almost all cases from a deletion within chromosome 22q11. We report the clinical findings in 44 cases. We propose that DiGeorge syndrome should be seen as the severe end of the clinical spectrum embraced by the acronym CATCH 22 syndrome; Cardiac defects, Abnormal facies, Thymic hypoplasia, Cleft palate, and Hypocalcaemia resulting from 22q11 deletions.
迪乔治综合征(DGS)包括胸腺发育不全、低钙血症、心脏流出道缺陷和面部畸形。几乎所有病例都是由22号染色体q11区域的缺失导致的。我们报告了44例患者的临床发现。我们认为迪乔治综合征应被视为由首字母缩写词CATCH 22综合征所涵盖的临床谱系的严重一端;即由22q11缺失导致的心脏缺陷、面部异常、胸腺发育不全、腭裂和低钙血症。