Skip to main content
Top
Published in: Archives of Gynecology and Obstetrics 1/2011

01-07-2011 | Short Communication

Antenatal three-dimensional sonographic features of Roberts syndrome

Authors: Daisy J. Dulnuan, Megumi Matsuoka, Emiko Uketa, Keiji Hayashi, Jun Murotsuki, Gen Nishimura, Toshiyuki Hata

Published in: Archives of Gynecology and Obstetrics | Issue 1/2011

Login to get access

Abstract

Introduction

We present a fetus whose characteristics most likely represent Roberts syndrome.

Case report

Prenatal diagnosis at 21 weeks and 1 day age of gestation was made employing conventional two-dimensional (2D) sonography, showing shortened upper and lower extremities. An umbilical cord cyst was also noted. Three-dimensional (3D) sonography revealed additional abnormalities which included bilateral hypoplastic and proximal implantation of the thumb, exophthalmic eyes, and suspected cleft lip. Shortened upper extremities, contracted legs, and an umbilical cord cyst were also clearly confirmed. Transparent X-ray mode uncovered the absence of radial and ulnar bones. Subtle fetal structures were readily discernible with 3D sonography so that the family could understand the fetal condition in utero. They underwent counseling, and opted for termination of the pregnancy. The sonographic findings were confirmed after delivery, supported by a 3D computed tomographic skeletal survey.

Conclusion

To the best of our knowledge, this is the first report of Roberts syndrome employing antenatal 3D sonographic imaging.
Literature
1.
go back to reference Stioui S, Priviteria O, Brambati B, Zuliani G, Lalatta F, Simoni G (1992) First-trimester prenatal diagnosis of Roberts Syndrome. Prenat Diagn 12:145–149PubMedCrossRef Stioui S, Priviteria O, Brambati B, Zuliani G, Lalatta F, Simoni G (1992) First-trimester prenatal diagnosis of Roberts Syndrome. Prenat Diagn 12:145–149PubMedCrossRef
2.
go back to reference Allington-Hawkins DJ, Tomskin DJ (1991) Somatic cell hybridization of Roberts syndrome and normal lymphoblast resulting in correction of both the cytogenetic and mutagen hypersensitivity cellular phenotypes. Som Cell Mol Genet 17:455–462CrossRef Allington-Hawkins DJ, Tomskin DJ (1991) Somatic cell hybridization of Roberts syndrome and normal lymphoblast resulting in correction of both the cytogenetic and mutagen hypersensitivity cellular phenotypes. Som Cell Mol Genet 17:455–462CrossRef
3.
go back to reference Rodriguez JI, Urioste M, Rodriguez-Peralto JL (1992) Tetraphocomelia with multiple malformations: X-linked Amelia or Roberts syndrome or DK-phocomelia syndrome? Am J Med Genet 43:630–631PubMedCrossRef Rodriguez JI, Urioste M, Rodriguez-Peralto JL (1992) Tetraphocomelia with multiple malformations: X-linked Amelia or Roberts syndrome or DK-phocomelia syndrome? Am J Med Genet 43:630–631PubMedCrossRef
4.
go back to reference Otano L, Matayoshi T, Gadow E (1996) Roberts syndrome: first-trimester prenatal diagnosis. Prenat Diagn 20:770–771CrossRef Otano L, Matayoshi T, Gadow E (1996) Roberts syndrome: first-trimester prenatal diagnosis. Prenat Diagn 20:770–771CrossRef
5.
go back to reference Feingold M (1994) History of C-Patient with SC-Roberts/pseudothalidomide syndrome. Am J Med Genet 43:898–899CrossRef Feingold M (1994) History of C-Patient with SC-Roberts/pseudothalidomide syndrome. Am J Med Genet 43:898–899CrossRef
6.
go back to reference Gruber A, Rabinerson D, Kaplan B, Ovadia Y (1994) Prenatal diagnosis of Roberts syndrome. Prenat Diagn 14:511–512PubMedCrossRef Gruber A, Rabinerson D, Kaplan B, Ovadia Y (1994) Prenatal diagnosis of Roberts syndrome. Prenat Diagn 14:511–512PubMedCrossRef
7.
go back to reference Benzacken B, Savary JB, Manouvrier S, Buccort M, Gonzales J (1996) Prenatal diagnosis of Roberts syndrome: two new cases. Prenat Diagn 16:125–130PubMedCrossRef Benzacken B, Savary JB, Manouvrier S, Buccort M, Gonzales J (1996) Prenatal diagnosis of Roberts syndrome: two new cases. Prenat Diagn 16:125–130PubMedCrossRef
8.
go back to reference Schulz S, Gerloff C, Ledig S, Langer D, Volleth M, Shirneshan K, Wieacker P (2008) Prenatal diagnosis of Roberts syndrome and detection of an ESCO2 frameshift mutation in a Pakistani family. Prenat Diagn 28:42–45PubMedCrossRef Schulz S, Gerloff C, Ledig S, Langer D, Volleth M, Shirneshan K, Wieacker P (2008) Prenatal diagnosis of Roberts syndrome and detection of an ESCO2 frameshift mutation in a Pakistani family. Prenat Diagn 28:42–45PubMedCrossRef
9.
go back to reference McDaniel LD, Prueitt R, Probst LC (2000) Novel assay for Roberts syndrome assigns variable phenotypes to one complementation group. Am J Med Genet 93:223–229PubMedCrossRef McDaniel LD, Prueitt R, Probst LC (2000) Novel assay for Roberts syndrome assigns variable phenotypes to one complementation group. Am J Med Genet 93:223–229PubMedCrossRef
10.
go back to reference Kennelly MM, Moran P (2007) A clinical algorithm of prenatal diagnosis of radial ray defects with two- and three-dimensional ultrasound. Prenat Diagn 27:730–737PubMedCrossRef Kennelly MM, Moran P (2007) A clinical algorithm of prenatal diagnosis of radial ray defects with two- and three-dimensional ultrasound. Prenat Diagn 27:730–737PubMedCrossRef
11.
go back to reference Leite JM, Granese R, Jeanty P, Herbst SS (2008) Fetal syndrome. In: Callen PW (ed) Ultrasonography in obstetrics and gynecology, 5th edn. Saunders Elsevier, Philadelphia, pp 166–180 Leite JM, Granese R, Jeanty P, Herbst SS (2008) Fetal syndrome. In: Callen PW (ed) Ultrasonography in obstetrics and gynecology, 5th edn. Saunders Elsevier, Philadelphia, pp 166–180
12.
go back to reference Grudy H, Burlbaw J, Walton S, Dannar C (1988) Robert syndrome: antenatal ultrasound—a case report. J Perinat Med 16:71–75CrossRef Grudy H, Burlbaw J, Walton S, Dannar C (1988) Robert syndrome: antenatal ultrasound—a case report. J Perinat Med 16:71–75CrossRef
13.
go back to reference Smith GN, Walker M, Johnston S, Ash K (1996) The sonographic finding of persistent umbilical cord cyst masses is associated with lethal aneuploidy and/or congenital anomalies. Prenat Diagn 16:141–147CrossRef Smith GN, Walker M, Johnston S, Ash K (1996) The sonographic finding of persistent umbilical cord cyst masses is associated with lethal aneuploidy and/or congenital anomalies. Prenat Diagn 16:141–147CrossRef
Metadata
Title
Antenatal three-dimensional sonographic features of Roberts syndrome
Authors
Daisy J. Dulnuan
Megumi Matsuoka
Emiko Uketa
Keiji Hayashi
Jun Murotsuki
Gen Nishimura
Toshiyuki Hata
Publication date
01-07-2011
Publisher
Springer-Verlag
Published in
Archives of Gynecology and Obstetrics / Issue 1/2011
Print ISSN: 0932-0067
Electronic ISSN: 1432-0711
DOI
https://doi.org/10.1007/s00404-011-1910-1

Other articles of this Issue 1/2011

Archives of Gynecology and Obstetrics 1/2011 Go to the issue

Materno-Fetal Medicine

The history of vaginal birth