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Dysgerminoma of the ovary in a patient with triple-X syndrome (47, XXX) and Marfanoid habitus features
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Affiliations- Department of Gynecology, Gynecologic Oncology and Gynecologic Endocrinology, Medical University of Gdansk, Poland
open access
Abstract
Abstract
Keywords
dysgerminoma; triple-X syndrome; Shprintzen-Goldberg syndrome; Marfan syndrome
About this articleTitle
Dysgerminoma of the ovary in a patient with triple-X syndrome (47, XXX) and Marfanoid habitus features
Journal
Issue
Article type
Clinical vignette
Pages
466-467
Published online
2021-05-20
Page views
840
Article views/downloads
604
DOI
Pubmed
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)- 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.
- 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.
- http://www.ncbi.nlm.nih.gov/omim/.
- Loeys BL, Dietz HC, Braverman AC, et al. The revised Ghent nosology for the Marfan syndrome. J Med Genet. 2010; 47(7): 476–485.
- 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.
