Pradel W, Bartsch O, Müller R, Lauer G, Eckelt U
Klinik und Poliklinik für Mund-, Kiefer- und Gesichtschirurgie, Universitätsklinikum Dresden.
HNO. 2003 Sep;51(9):755-8. doi: 10.1007/s00106-003-0874-2.
The DiGeorge syndrome/velocardiofacial syndrome is the most frequent chromosomal microdeletion syndrome. Partial deletion of chromosome 22q11 may lead to symptoms including facial dysmorphy, hypoparathyroidism, thymic aplasia, congenital heart disease, developmental retardation, and disturbance of speech development. According to the literature, 9% of patients have cleft palate, an additional 5% have a submucosal cleft, and a total of 32% show velopharyngeal insufficiency. We studied 64 children with a cleft, or with delayed speech development and a submucosal or occult cleft, for the presence of the 22q11deletion using fluorescent in situ hybridisation. Five patients had the 22q11 deletion. We conclude that patients presenting with nasal speech and additional anomalies should all be studied for the presence of submucosal or occult clefting and for the presence of the DiGeorge syndrome/velocardiofacial syndrome.
迪乔治综合征/腭心面综合征是最常见的染色体微缺失综合征。22q11染色体部分缺失可能导致面部畸形、甲状旁腺功能减退、胸腺发育不全、先天性心脏病、发育迟缓以及言语发育障碍等症状。根据文献记载,9%的患者患有腭裂,另有5%患有黏膜下腭裂,总计32%表现为腭咽功能不全。我们使用荧光原位杂交技术对64例患有腭裂、或言语发育迟缓以及黏膜下或隐性腭裂的儿童进行了22q11缺失情况的研究。5例患者存在22q11缺失。我们得出结论,对于出现鼻音以及其他异常情况的患者,均应进行黏膜下或隐性腭裂以及迪乔治综合征/腭心面综合征的检查。