Matsuoka R, Takao A, Kimura M, Imamura S, Kondo C, Joh-o K, Ikeda K, Nishibatake M, Ando M, Momma K
Department of Pediatric Cardiology, Tokyo Women's Medical College, Japan.
Am J Med Genet. 1994 Nov 15;53(3):285-9. doi: 10.1002/ajmg.1320530314.
The so-called "conotruncal anomaly face syndrome" (CTAFS) is characterized by a peculiar facial appearance associated with congenital heart disease (CHD), especially cardiac outflow tract defects such as tetralogy of Fallot (TOF), double outlet right ventricle (DORV), and truncus arteriosus (TAC). CTAFS and the DiGeorge anomaly (DGA) have many similar phenotypic characteristics, suggesting that they share a common cause. In many cases DGA is known to be associated with monosomy for a region of chromosome 22q11.2. Fifty CTAFS patients and 10 DGA patients, 11 parents couples and 10 mothers of CTAFS patients, and 3 parents couples and 2 mothers of DGA patients were examined by fluorescent in situ hybridization (FISH) using the N25 (D22S75) DGCR probe (Oncor). Monosomy for a region of 22q11.2 was found in 42 CTAFS, 9 DGA, 4 mothers, and 1 father who had CTAF without CHD. The remaining 8 CTAFS patients 1 DGA patient and 1 mother who had questionable CTAF without CHD, showed no such chromosome abnormality. For the control, 60 patients who had CHD without CTAF or other known malformation syndromes were examined and had no deletion of 22q11.2. Therefore, we conclude that CTAFS is a part of the CATCH 22 syndrome; cardiac defects, abnormal faces, thymic hypoplasia, cleft palate, and hypocalcemia (CATCH) resulting from 22q11.2 deletions.
所谓的“圆锥动脉干异常面容综合征”(CTAFS)的特征是具有与先天性心脏病(CHD)相关的特殊面容,尤其是心脏流出道缺陷,如法洛四联症(TOF)、右心室双出口(DORV)和动脉干永存(TAC)。CTAFS和迪乔治异常(DGA)有许多相似的表型特征,表明它们有共同的病因。在许多病例中,已知DGA与22q11.2染色体区域的单体性相关。使用N25(D22S75)DGCR探针(Oncor)通过荧光原位杂交(FISH)对50例CTAFS患者和10例DGA患者、11对父母以及10例CTAFS患者的母亲、3对父母以及2例DGA患者的母亲进行了检查。在42例CTAFS患者、9例DGA患者、4例母亲以及1例无CHD的CTAF患者父亲中发现了22q11.2区域的单体性。其余8例CTAFS患者、1例DGA患者以及1例无CHD的可疑CTAF患者的母亲未显示出此类染色体异常。作为对照,对60例无CTAF或其他已知畸形综合征的CHD患者进行了检查,未发现22q11.2缺失。因此,我们得出结论,CTAFS是22q11.2缺失导致的心脏缺陷、面容异常、胸腺发育不全、腭裂和低钙血症(CATCH)22综合征的一部分。