open access

Vol 92, No 6 (2021)
Clinical vignette
Published online: 2021-05-20
Get Citation

Dysgerminoma of the ovary in a patient with triple-X syndrome (47, XXX) and Marfanoid habitus features

Karolina Moskwinska1, Marcin Sniadecki1, Dariusz Wydra1
DOI: 10.5603/GP.a2021.0106
·
Pubmed: 34105760
·
Ginekol Pol 2021;92(6):466-467.
Affiliations
  1. Department of Gynecology, Gynecologic Oncology and Gynecologic Endocrinology, Medical University of Gdansk, Poland

open access

Vol 92, No 6 (2021)
CLINICAL VIGNETTES
Published online: 2021-05-20

Abstract

Not available

Abstract

Not available
Get Citation

Keywords

dysgerminoma; triple-X syndrome; Shprintzen-Goldberg syndrome; Marfan syndrome

About this article
Title

Dysgerminoma of the ovary in a patient with triple-X syndrome (47, XXX) and Marfanoid habitus features

Journal

Ginekologia Polska

Issue

Vol 92, No 6 (2021)

Article type

Clinical vignette

Pages

466-467

Published online

2021-05-20

DOI

10.5603/GP.a2021.0106

Pubmed

34105760

Bibliographic record

Ginekol Pol 2021;92(6):466-467.

Keywords

dysgerminoma
triple-X syndrome
Shprintzen-Goldberg syndrome
Marfan syndrome

Authors

Karolina Moskwinska
Marcin Sniadecki
Dariusz Wydra

References (5)
  1. Feenstra I, Fang J, Koolen DA, et al. European Cytogeneticists Association Register of Unbalanced Chromosome Aberrations (ECARUCA); an online database for rare chromosome abnormalities. Eur J Med Genet. 2006; 49(4): 279–291.
  2. Firth HV, Richards SM, Bevan AP, et al. DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources. Am J Hum Genet. 2009; 84(4): 524–533.
  3. http://www.ncbi.nlm.nih.gov/omim/.
  4. Loeys BL, Dietz HC, Braverman AC, et al. The revised Ghent nosology for the Marfan syndrome. J Med Genet. 2010; 47(7): 476–485.
  5. Shprintzen RJ, Goldberg RB. A recurrent pattern syndrome of craniosynostosis associated with arachnodactyly and abdominal hernias. J Craniofac Genet Dev Biol. 1982; 2(1): 65–74.

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