Clinical Manifestations of Partial Trisomy 4p

Author:

Demirhan O1,Özgünen F2,Taştemir D3

Affiliation:

1. Department of Medical Biology and Genetics, Faculty of Medicine, Çukurova University, Adana, Turkey1

2. Department of Gynecology and Obstetrics, Faculty of Medicine, Çukurova University, Adana, Turkey2

3. Vocational School of Health Services, Adıyaman University, Adıyaman, Turkey3

Abstract

Clinical Manifestations of Partial Trisomy 4pWe made the diagnosis prenatally from cytogenetic analysis of amniocytes cultured following amniocentesis performed at 20 weeks' gestation on a woman in whom ultrasound examination of the female fetus showed severe growth retardation, lung and kidney hypoplasia, and a congenital heart defect. Analysis revealed a de novo trisomy of the terminal short arm of chromosome 4 (4p16.1-pter). The parents opted to terminate the pregnancy. Fetopathological examination showed dysmorphic features and other abnormalities consistent with clinical manifestations of partial trisomy 4p.

Publisher

Walter de Gruyter GmbH

Subject

Genetics (clinical),Genetics

Reference12 articles.

1. Inherited pericentric inversion of chromosome no. 4;M. Wilson;Am J Hum Genet,1970

2. Trisomy of the short arm of chromosome 4: the changing phenotype with age;A. Kleczkowska;Ann Genet,1992

3. Trisomy 4p: five new observations and overview;B. Dallapiccola;Clin Genet,1977

4. The trisomy 4p syndrome: case report and review;C. Gonzalez;Am J Med Genet,1977

5. Partial monosomy Xq(Xq23-qter) and trisomy 4p(4p15.33-pter) in a woman with intractable focal epilepsy, borderline intellectual functioning and dysmorphic features;A. Bartocci;Brain Dev,2008

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Partial Trisomy 4p Syndrome Diagnosed Prenatally;Fetal and Pediatric Pathology;2023-11-10

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