Klippel–Trenaunay syndrome belongs to the PIK3CA‐related overgrowth spectrum (PROS)
Article Properties
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LanguageEnglish
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DOI (url)
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Publication Date2015/10/13
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Journal
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Indian UGC (journal)
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Refrences45
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Citations125
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Hassan Vahidnezhad Department of Dermatology and Cutaneous Biology The Sidney Kimmel Medical College at Thomas Jefferson University Philadelphia PA USAMolecular Medicine Division Biotechnology Research Center Pasteur Institute of Iran Tehran Iran
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Leila Youssefian Department of Dermatology and Cutaneous Biology The Sidney Kimmel Medical College at Thomas Jefferson University Philadelphia PA USADepartment of Medical Genetics School of Medicine Tehran University of Medical Sciences Tehran Iran
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Jouni Uitto Department of Dermatology and Cutaneous Biology The Sidney Kimmel Medical College at Thomas Jefferson University Philadelphia PA USA
Abstract
Cite
Vahidnezhad, Hassan, et al. “Klippel–Trenaunay Syndrome Belongs to the PIK3CA‐related Overgrowth Spectrum (PROS)”. Experimental Dermatology, vol. 25, no. 1, 2015, pp. 17-19, https://doi.org/10.1111/exd.12826.
Vahidnezhad, H., Youssefian, L., & Uitto, J. (2015). Klippel–Trenaunay syndrome belongs to the PIK3CA‐related overgrowth spectrum (PROS). Experimental Dermatology, 25(1), 17-19. https://doi.org/10.1111/exd.12826
Vahidnezhad, Hassan, Leila Youssefian, and Jouni Uitto. “Klippel–Trenaunay Syndrome Belongs to the PIK3CA‐related Overgrowth Spectrum (PROS)”. Experimental Dermatology 25, no. 1 (2015): 17-19. https://doi.org/10.1111/exd.12826.
Vahidnezhad H, Youssefian L, Uitto J. Klippel–Trenaunay syndrome belongs to the PIK3CA‐related overgrowth spectrum (PROS). Experimental Dermatology. 2015;25(1):17-9.
Journal Categories
Medicine
Dermatology
Medicine
Medicine (General)
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Refrences
| Title | Journal | Journal Categories | Citations | Publication Date |
|---|---|---|---|---|
Somatic mosaicism for the p.His1047Arg mutation in PIK3CA in a girl with mesenteric lipomatosis | American Journal of Medical Genetics Part A |
| 12 | 2014 |
| Somatic mosaicism for the p.His1047Arg mutation in PIK3CA in a girl with mesenteric lipomatosis | 2014 | |||
| Somatic mosaicism for the p.His1047Arg mutation in PIK3CA in a girl with mesenteric lipomatosis | 1900 | |||
| 10.1002/(SICI)1096-8628(19970502)70:1<67::AID-AJMG13>3.0.CO;2-V | ||||
| Macrocephaly with cutis marmorata, haemangioma and syndactyly ??? a distinctive overgrowth syndrome | Clinical Dysmorphology |
| 92 | 1997 |
Citations
| Title | Journal | Journal Categories | Citations | Publication Date |
|---|---|---|---|---|
| Diseases of the blood vessels and thrombosis | Surgery (Oxford) | 2024 | ||
| Sirolimus for vascular anomalies in the first year of life: a systematic review | Journal of Perinatology |
| 2024 | |
| Research Progress on the Genetics of CLOVES Syndrome and the Identification of Related Diseases | Advances in Clinical Medicine | 2024 | ||
A Rare Case of Klippel Trenaunay Syndrome with Von Willebrand Factor Deficiency and Multiple Accessory Spleens: A Case Report and Brief Literature Review | Advanced Biomedical Research |
| 2024 | |
A rare presentation of pupillary block glaucoma and persistent tunica vasculosa lentis in Klippel–Trenaunay syndrome | Indian Journal of Ophthalmology - Case Reports | 2024 |
Citations Analysis
The category
Medicine: Medicine (General) 81
is the most commonly referenced area in studies that cite this article. The first research to cite this article was titled Copy number variants in a population‐based investigation of Klippel–Trenaunay syndrome and was published in 2016. The most recent citation comes from a 2024 study titled Research Progress on the Genetics of CLOVES Syndrome and the Identification of Related Diseases. This article reached its peak citation in 2022, with 25 citations. It has been cited in 98 different journals, 27% of which are open access. Among related journals, the Journal of the European Academy of Dermatology and Venereology cited this research the most, with 3 citations. The chart below illustrates the annual citation trends for this article.