A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation

被引:3
作者
Chen, Chih-Ping [1 ,2 ,3 ,4 ,5 ,6 ]
Lin, Shuan-Pei [2 ,7 ,8 ,9 ]
Chern, Schu-Rern [2 ]
Wu, Peih-Shan [10 ]
Su, Jun-Wei [1 ,11 ]
Lee, Chen-Chi [1 ]
Wang, Wayseen [2 ,12 ]
机构
[1] Mackay Mem Hosp, Dept Obstet & Gynecol, Taipei, Taiwan
[2] Mackay Mem Hosp, Dept Med Res, Taipei, Taiwan
[3] Asia Univ, Dept Biotechnol, Taichung, Taiwan
[4] China Med Univ, Coll Chinese Med, Sch Chinese Med, Taichung, Taiwan
[5] Natl Yang Ming Univ, Inst Clin & Community Hlth Nursing, Taipei 112, Taiwan
[6] Natl Yang Ming Univ, Sch Med, Dept Obstet & Gynecol, Taipei 112, Taiwan
[7] Mackay Med Coll, Dept Med, New Taipei City, Taiwan
[8] Mackay Mem Hosp, Dept Pediat, Taipei, Taiwan
[9] Mackay Jr Coll Med Nursing & Management, Taipei, Taiwan
[10] Gene Biodesign Co Ltd, Taipei, Taiwan
[11] China Med Univ Hosp, Dept Obstet & Gynecol, Taichung, Taiwan
[12] Tatung Univ, Dept Bioengn, Taipei 104, Taiwan
来源
TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY | 2014年 / 53卷 / 01期
关键词
12p11.22-p11.21; deletion; 22q11.2; duplication; autism; DDX11; BALANCED RECIPROCAL TRANSLOCATIONS; MICRODUPLICATION; 22Q11.2; IDENTIFICATION; ASSOCIATION; DISORDER; MUTATION; HELICASE; DDX11; CHLR1; CHILD;
D O I
10.1016/j.tjog.2013.10.037
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To present an array comparative genomic hybridization (aCGH) characterization of a 12p11.22 -p11.21 microdeletion and 22q11.2 microduplication in an adolescent girl with autism, mental retardation, facial dysmorphism, microcephaly, behavior problems, and an apparently balanced reciprocal translocation of t(8;12)(q243;p11.2). Materials and methods: A 13-year-old girl was referred to the hospital because of autism, mental retardation, and difficulty in the self-care of her menstruation. Cytogenetic analysis revealed an apparently balanced reciprocal translocation and a karyotype of 46,XX,t(8;12) (q243;p11.2)dn. The girl manifested microcephaly, hypertelorism, flat facial profile, prominent forehead, thick scalp hair, upslanting palpebral fissures, broad nasal bridge, bulbous nose, right simian crease, bilateral clinodactyly of the fifth fingers, bilateral pes cavus, learning difficulties, mental retardation, emotional instability, cognitive impairment, behavior problems, jumping-like gaits, and autistic spectrum disorder. aCGH was performed to evaluate genomic imbalance in this patient. Results: aCGH analysis revealed a 137-Mb 12p11.22-p11.21 microdeletion or arr [hg 19] 12p11.22-p11.21 (30,645,008-32,014,774) x 1 and a 367-kb 22q11.21 microduplication or arr [hg 19] 22q11.21 (18,657,470 -19,024,306) x 3. The 1.37-Mb 12p11.22-p11.21 microdeletion encompassed 26 genes including IPO8, CAPRIN2, and DDX11, and the 367-kb 22q11.21 microduplication encompassed 20 genes including USP18, DGCR6, PRODH, and DGCR2. Conclusion: An apparently balanced translocation may be in fact affected by concurrent deletion and duplication in two different chromosomal regions. Our presentation provides information on diagnostic phenotype of 12p11.22-p1121 microdeletion and 22q112 microduplication. Copyright (C) 2014, Taiwan Association of Obstetrics & Gynecology. Published by Elsevier Taiwan LLC. All rights reserved.
引用
收藏
页码:74 / 78
页数:5
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