Literature DB >> 11555459

Prenatal ultrasound findings in a fetus with paternal uniparental disomy 14q12-qter.

D Towner1, S P Yang, L G Shaffer.   

Abstract

We present the prenatal ultrasound findings in a case of postnatally identified paternal uniparental isodisomy 14q12-qter. Increased nuchal translucency and a large omphalocele were identified at 14 weeks' gestation. Karyotyping revealed a normal male, 46,XY. As gestation advanced, polyhydramnios developed, skeletal abnormalities involving the long bones and chest became evident, hand contractures developed, and the presumed large omphalocele was in part found to be a large ventral hernia, as echogenic adipose tissue could be seen in the abdominal wall near to the cord insertion. Prenatal findings were confirmed after delivery and central nervous system imaging revealed lissencephaly. The combination of an abdominal wall defect with either increased nuchal translucency or skeletal abnormalities should prompt an investigation for uniparental disomy 14 even if the karyotype is normal.

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Year:  2001        PMID: 11555459     DOI: 10.1046/j.1469-0705.2001.00451.x

Source DB:  PubMed          Journal:  Ultrasound Obstet Gynecol        ISSN: 0960-7692            Impact factor:   7.299


  6 in total

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Authors:  Alberto L Rosa; Yuan-Qing Wu; Bernard Kwabi-Addo; Karen J Coveler; V Reid Sutton; Lisa G Shaffer
Journal:  Chromosome Res       Date:  2005-12-08       Impact factor: 5.239

2.  Radiological evaluation of dysmorphic thorax of paternal uniparental disomy 14.

Authors:  Osamu Miyazaki; Gen Nishimura; Masayo Kagami; Tsutomu Ogata
Journal:  Pediatr Radiol       Date:  2011-05-24

3.  Genome-wide prediction of imprinted murine genes.

Authors:  Philippe P Luedi; Alexander J Hartemink; Randy L Jirtle
Journal:  Genome Res       Date:  2005-06       Impact factor: 9.043

4.  Paternal uniparental disomy for chromosome 14: prenatal management.

Authors:  Joana Isabel Igreja da Silva; Barbara Ribeiro; Alexandra Cadilhe; Cristina Nogueira-Silva
Journal:  BMJ Case Rep       Date:  2019-12-30

5.  Kagami-Ogata Syndrome: Case Series and Review of Literature.

Authors:  Rishika P Sakaria; Roya Mostafavi; Stephen Miller; Jewell C Ward; Eniko K Pivnick; Ajay J Talati
Journal:  AJP Rep       Date:  2021-05-27

6.  Case report: Prenatal diagnosis of Kagami-Ogata syndrome in a Chinese family.

Authors:  Junjie Hu; Ying Zhang; Yanmei Yang; Liya Wang; Yixi Sun; Minyue Dong
Journal:  Front Genet       Date:  2022-08-11       Impact factor: 4.772

  6 in total

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