Prenatal diagnosis of familial 3p26.3p25.3 deletion in a pregnancy associated with a favorable fetal outcome and asymptomatic carrier parent and family members in three generations

被引:0
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作者
Chen, Chih-Ping [1 ,2 ,3 ,4 ,5 ,6 ]
Wu, Fang-Tzu [1 ]
Pan, Yen-Ting [1 ]
Wu, Peih-Shan [7 ]
Lee, Meng-Shan [1 ]
Wang, Wayseen [2 ]
机构
[1] Mackay Mem Hosp, Dept Obstet & Gynecol, 92,Sect 2,Chung Shan North Rd, Taipei 10449, Taiwan
[2] Mackay Mem Hosp, Dept Med Res, Taipei 10449, Taiwan
[3] China Med Univ, Coll Chinese Med, Sch Chinese Med, Taichung, Taiwan
[4] Natl Yang Ming Chiao Tung Univ, Inst Clin & Community Hlth Nursing, Taipei, Taiwan
[5] Natl Yang Ming Chiao Tung Univ, Sch Med, Dept Obstet & Gynecol, Taipei, Taiwan
[6] Asia Univ, Coll Med & Hlth Sci, Dept Med Lab Sci & Biotechnol, Taichung, Taiwan
[7] Gene Biodesign Co Ltd, Taipei, Taiwan
来源
关键词
3p26.3p25.3; deletion; Distal 3p deletion; Prenatal diagnosis; PARTIAL MONOSOMY 3P; INTELLECTUAL DISABILITY; DYSMORPHIC FEATURES; MUTATIONS; PHENOTYPE; MOTHER; 3P25.3; SETD5; PTER;
D O I
10.1016/j.tjog.2024.05.010
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Objective: We present prenatal diagnosis of familial 3p26.3p25.3 deletion in a pregnancy associated with a favorable fetal outcome and asymptomatic carrier parent and family members in three generations. Case Report: A 35-year-old, gravida 2, para 1, woman underwent amniocentesis at 17 weeks of gestation because of advanced maternal age and the carrier of distal 3p deletion. She was phenotypically normal, and there was no family history of congenital anomalies. Amniocentesis revealed a karyotype of 46,XY,del(3)(p26.1). Repeat amniocentesis at 21 weeks of gestation revealed a karyotype of 46,XY,del(3)(p25.3). Simultaneous array comparative genomic hybridization (aCGH) analysis on the DNA extracted from uncultured amniocytes showed the result of arr 3p26.3p25.3 (117,735-8,709,972) x 1.0 [GRCh37 (hg19)] with an 8.59-Mb deletion of 3p26.3p25.3 encompassing 14 OMIM genes of CHL1, CNTN6, CNTN4, IL5RA, TRNT1, CRBN, SETMAR, SUMF1, ITPR1, BHLHE40, ARL8B, GRM7, LMCD1 and SSUH2. Cytogenetic analysis of parental bloods revealed a karyotype of 46,XX,del (3) (p25.3) in the mother and 46,XY in the father. The woman's 69-year-old mother and her 2-year-old elder son carried the same aberrant chromosome of 3p25.3/p26.3 deletion by conventional cytogenetic analysis but manifested no phenotypic abnormality. aCGH analysis of the peripheral bloods showed that the woman's mother and her elder son had the same 8.59-Mb deletion of 3p26.3p25.3. The woman was advised to continue the pregnancy. At 39 weeks of gestation, a 3040-g healthy male baby was delivered. When follow-up at age 21/2 1 / 2 years, the neonate was normal in development and showed no apparent phenotypic abnormality. Conclusion: Distal 3p deletion of 3p26.3p25.3 involving the OMIM genes from CHL1 to SSUH2 can be associated with no apparent phenotypic abnormality. (c) 2024 Taiwan Association of Obstetrics & Gynecology. Publishing services by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:561 / 564
页数:4
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