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Clinical vignette
Published online: 2021-05-20
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Dysgerminoma of the ovary in a patient with triple-X syndrome (47, XXX) and Marfanoid habitus features

Karolina Moskwinska, Marcin Sniadecki, Dariusz Wydra
DOI: 10.5603/GP.a2021.0106
·
Pubmed: 34105760

open access

Ahead of Print
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

Ahead of Print

Article type

Clinical vignette

Published online

2021-05-20

DOI

10.5603/GP.a2021.0106

Pubmed

34105760

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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