Chromosome 1p32-p31 deletion syndrome: Prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction

被引:25
|
作者
Chen, Chih-Ping [1 ,2 ,3 ,4 ,5 ,6 ]
Su, Yi-Ning [7 ]
Chen, Yi-Yung [1 ]
Chern, Schu-Rern [2 ]
Liu, Yu-Peng [8 ,9 ]
Wu, Pei-Chen [1 ]
Lee, Chen-Chi [1 ]
Chen, Yu-Ting [2 ]
Wang, Wayseen [2 ,10 ]
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, Dept Obstet & Gynecol, Sch Med, Taipei 112, Taiwan
[7] Natl Taiwan Univ Hosp, Dept Med Genet, Taipei, Taiwan
[8] Mackay Mem Hosp, Hsinchu Branch, Dept Radiol, Hsinchu, Taiwan
[9] Mackay Med Nursing & Management Coll, Taipei, Taiwan
[10] Tatung Univ, Dept Bioengn, Taipei 104, Taiwan
来源
关键词
Abnormal external genitalia; Chromosome 1p32-p31 deletion syndrome; Corpus callosum hypogenesis; Ventriculomegaly; NUCLEAR FACTOR-I; SEVERE MENTAL-RETARDATION; ANEUPLOIDY DIAGNOSIS; AGENESIS; HYDROCEPHALUS; MALFORMATIONS; TRANSLOCATION; MICRODELETION; FOREBRAIN; PREGNANCY;
D O I
10.1016/j.tjog.2011.07.014
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To present prenatal diagnosis of chromosome 1p32-p31 deletion syndrome with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction and to review the literature. Materials, Methods, and Results: A 26-year-old, primigravid woman was referred for amniocentesis at 30 weeks of gestation because of hydrocephalus and short limbs. Prenatal ultrasound showed macrocephaly, prominent forehead, ventriculomegaly, corpus callosum hypogenesis, micrognathia, and ambiguous external genitalia. Amniocentesis was performed, and array comparative genomic hybridization using uncultured amniocytes revealed a 22.2-Mb deletion of 1p32.3-p31.1 [arr cgh 1p32.3p31.1 (55,500,291 bp-77,711,982 bp)x 1] encompassing the genes of NFIA. GPR177, and 89 additional genes. Cytogenetic analysis revealed a karyotype of 46,XX,del(I)(p31.1p32.3)dn. At 33 weeks of gestation, a dead fetus was delivered with a body weight of 1536 g (<5(th) centile); relative macrocephaly; a broad face; prominent forehead; hypertelorism; anteverted nostrils; micrognathia; low-set ears; and abnormal female external genitalia with labial fusion, labial hypertrophy, absence of vaginal opening, and clitoral hypertrophy. Polymorphic DNA marker analysis determined a paternal origin of the deletion. Conclusion: Prenatal diagnosis of ventriculomegaly with an abnormal corpus callosum should alert subtle chromosome aberrations and prompt molecular cytogenetic investigation if necessary. Fetuses with chromosome 1p32-p31 deletion syndrome and haploinsufficiency of the NFIA gene may present ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction in the third trimester. Copyright (C) 2011, Taiwan Association of Obstetrics & Gynecology. Published by Elsevier Taiwan LLC. All rights reserved.
引用
收藏
页码:345 / 352
页数:8
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