Literature DB >> 19372699

Increased nuchal translucency and other ultrasound findings in a case of simpson-golabi-behmel syndrome.

Chumei C Li1, Sarah D McDonald.   

Abstract

OBJECTIVES: Fetal imaging, in particular nuchal translucency, is playing an increasingly important role in diagnosing genetic syndromes. We report imaging findings of a male fetus with Simpson-Golabi-Behmel (SGB) syndrome. METHODS AND
RESULTS: The SGB case was noted to have increased nuchal translucency on integrated prenatal screening, in conjunction with elevated maternal serum alpha fetal protein and body wall edema. Subsequent ultrasound findings at 30 weeks gestation included polyhydramnios, macrosomia, macroglossia, left-sided cleft lip and palate, nephromegaly, hepatosplenomegaly as well as an abnormal skull shape due to lamboid craniosynostosis.
CONCLUSIONS: To our knowledge this is the first case report of increased nuchal translucency and craniosynostosis associated with SGB syndrome. A mutation in the glypican-3 gene was found in both the proband and the mother, who is a manifesting carrier. Copyright (c) 2009 S. Karger AG, Basel.

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Year:  2008        PMID: 19372699     DOI: 10.1159/000213487

Source DB:  PubMed          Journal:  Fetal Diagn Ther        ISSN: 1015-3837            Impact factor:   2.587


  7 in total

1.  Transient QT interval prolongation in an infant with Simpson-Golabi-Behmel syndrome.

Authors:  Emily Gertsch; Salman Kirmani; Michael J Ackerman; Dusica Babovic-Vuksanovic
Journal:  Am J Med Genet A       Date:  2010-09       Impact factor: 2.802

2.  Two Consecutive Pregnancies with Simpson-Golabi-Behmel Syndrome Type 1: Case Report and Review of Published Prenatal Cases.

Authors:  Konstantin Ridnõi; Elvira Kurvinen; Sander Pajusalu; Tiia Reimand; Katrin Õunap
Journal:  Mol Syndromol       Date:  2018-06-08

3.  A prenatal case of Simpson-Golabi-Behmel syndrome type 1 with a 0.26-Mb deletion fragment at Xq26.2 inherited from mother: Case report.

Authors:  Jing Sha; Fangfang Tan; Ying Liu; Zaochun Xu; Xuezhen Wang; Jingfang Zhai
Journal:  Medicine (Baltimore)       Date:  2022-04-22       Impact factor: 1.817

Review 4.  Simpson-Golabi-Behmel syndrome types I and II.

Authors:  Jair Tenorio; Pedro Arias; Víctor Martínez-Glez; Fernando Santos; Sixto García-Miñaur; Julián Nevado; Pablo Lapunzina
Journal:  Orphanet J Rare Dis       Date:  2014-09-20       Impact factor: 4.123

5.  First reported case of Simpson-Golabi-Behmel syndrome in a female fetus diagnosed prenatally with chromosomal microarray.

Authors:  Heidi Kristine Støve; Naja Becher; Vibike Gjørup; Mette Ramsing; Ida Vogel; Else Marie Vestergaard
Journal:  Clin Case Rep       Date:  2017-03-17

6.  Whole exome sequencing aids the diagnosis of Simpson-Golabi-Behmel syndrome in two male fetuses.

Authors:  Jingjing Xiang; Qin Zhang; Xiaoyan Song; Yinghua Liu; Haibo Li; Hong Li; Ting Wang
Journal:  J Int Med Res       Date:  2019-07-15       Impact factor: 1.671

Review 7.  Prenatal case of Simpson-Golabi-Behmel syndrome with a de novo 370Kb-sized microdeletion of Xq26.2 compassing partial GPC3 gene and review.

Authors:  Jing Liu; Qin Liu; Shuting Yang; Na Ma; Jialun Pang; Ying Peng; Hui Xi; Zhengjun Jia; Yingchun Luo; Meiping Jiang; Yanling Teng; Wenxian Yu; Zhuo Li; Hua Wang
Journal:  Mol Genet Genomic Med       Date:  2021-07-22       Impact factor: 2.183

  7 in total

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