Partial Trisomy 4p Syndrome Diagnosed Prenatally.

IF 0.7 4区 医学 Q4 PATHOLOGY Fetal and Pediatric Pathology Pub Date : 2024-03-01 Epub Date: 2023-11-10 DOI:10.1080/15513815.2023.2279138
Kaouther Nasri, Nadia Ben Jamaa, Ines Ouertani, Nadia Boujelben
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Abstract

Introduction: Trisomy 4p is a lethal chromosomal disorder, resulting from segmental or full trisomy of the short arm of chromosome 4. Prenatal diagnosis may allow decisions on whether to continue or terminate the pregnancy. Case report: We diagnosed a fetus with partial trisomy 4p after first-trimester ultrasound detection of increased nuchal translucency, allowing the parents the opportunity to terminate the pregnancy. The partial trisomy 4p was inherited from a balanced translocation carried by the father. Discussion/Conclusion: For this family, the risk of unbalanced chromosomal alterations in subsequent pregnancies is increased due to the father's translocation. Appropriate genetic counseling with future prenatal diagnosis through amniocentesis can be offered to the couple. Trisomy 4p can be associated with increased nuchal thickness in the first trimester.

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产前诊断的部分三体4p综合征。
引言:4p三体是一种致命的染色体疾病,由4号染色体短臂的节段或全三体引起。产前诊断可以决定是继续妊娠还是终止妊娠。病例报告:我们在孕早期超声检测到胎儿颈部半透明性增加后,诊断出胎儿为部分性4p三体,使父母有机会终止妊娠。4p部分三体是由父亲携带的平衡易位遗传的。讨论/结论:对于这个家庭来说,由于父亲的易位,在随后的妊娠中染色体不平衡改变的风险增加。可以为这对夫妇提供适当的基因咨询,并在未来通过羊水穿刺进行产前诊断。4p三体可能与妊娠早期珠心厚度增加有关。
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来源期刊
CiteScore
3.00
自引率
0.00%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Fetal and Pediatric Pathology is an established bimonthly international journal that publishes data on diseases of the developing embryo, newborns, children, and adolescents. The journal publishes original and review articles and reportable case reports. The expanded scope of the journal encompasses molecular basis of genetic disorders; molecular basis of diseases that lead to implantation failures; molecular basis of abnormal placentation; placentology and molecular basis of habitual abortion; intrauterine development and molecular basis of embryonic death; pathogenisis and etiologic factors involved in sudden infant death syndrome; the underlying molecular basis, and pathogenesis of diseases that lead to morbidity and mortality in newborns; prenatal, perinatal, and pediatric diseases and molecular basis of diseases of childhood including solid tumors and tumors of the hematopoietic system; and experimental and molecular pathology.
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