Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2009 1
2010 2
2012 2
2013 1
2014 5
2015 3
2016 5
2017 5
2018 2
2019 2
2020 1
2021 5
2022 8
2023 1
2024 2

Text availability

Article attribute

Article type

Publication date

Search Results

37 results

Results by year

Filters applied: . Clear all
Page 1
Capillary Malformations.
Escobar K, Pandher K, Jahnke MN. Escobar K, et al. Dermatol Clin. 2022 Oct;40(4):425-433. doi: 10.1016/j.det.2022.06.005. Epub 2022 Sep 16. Dermatol Clin. 2022. PMID: 36243429 Review.
Some genetic disorders discussed, which feature CMs, include Sturge-Weber syndrome, diffuse CMs with overgrowth, Klippel-Trenaunay syndrome, CLOVES syndrome, among others. This article can aid clinicians in better identifying CMs and associated syndromes and provide …
Some genetic disorders discussed, which feature CMs, include Sturge-Weber syndrome, diffuse CMs with overgrowth, Klippel-Trenaunay syndrome, …
PIK3CA-related overgrowth spectrum (PROS): diagnostic and testing eligibility criteria, differential diagnosis, and evaluation.
Keppler-Noreuil KM, Rios JJ, Parker VE, Semple RK, Lindhurst MJ, Sapp JC, Alomari A, Ezaki M, Dobyns W, Biesecker LG. Keppler-Noreuil KM, et al. Am J Med Genet A. 2015 Feb;167A(2):287-95. doi: 10.1002/ajmg.a.36836. Epub 2014 Dec 31. Am J Med Genet A. 2015. PMID: 25557259 Free PMC article.
Historically, the clinical diagnoses in patients with PIK3CA activating mutations have included Fibroadipose hyperplasia or Overgrowth (FAO), Hemihyperplasia Multiple Lipomatosis (HHML), Congenital Lipomatous Overgrowth, Vascular Malformations, Epidermal Nevi, Scoliosis/Skeletal …
Historically, the clinical diagnoses in patients with PIK3CA activating mutations have included Fibroadipose hyperplasia or Overgrowth (FAO) …
CLOVES syndrome.
Bloom J, Upton J 3rd. Bloom J, et al. J Hand Surg Am. 2013 Dec;38(12):2508-12. doi: 10.1016/j.jhsa.2013.08.120. Epub 2013 Oct 23. J Hand Surg Am. 2013. PMID: 24161472 Review.
Although hand anomalies alone cannot make the diagnosis, the foot, truncal, cutaneous and spinal anomalies are particularly diagnostic. CLOVES syndrome has emerged as a distinct clinical entity diagnosed by clinical and radiographic examinations. ...
Although hand anomalies alone cannot make the diagnosis, the foot, truncal, cutaneous and spinal anomalies are particularly diagnostic. C …
CLOVES syndrome: review of a PIK3CA-related overgrowth spectrum (PROS).
Martinez-Lopez A, Blasco-Morente G, Perez-Lopez I, Herrera-Garcia JD, Luque-Valenzuela M, Sanchez-Cano D, Lopez-Gutierrez JC, Ruiz-Villaverde R, Tercedor-Sanchez J. Martinez-Lopez A, et al. Clin Genet. 2017 Jan;91(1):14-21. doi: 10.1111/cge.12832. Epub 2016 Aug 3. Clin Genet. 2017. PMID: 27426476 Review.
Identification of the clinical and genetic characteristics of CLOVES syndrome is crucial for the differential diagnosis with other overgrowth syndromes, such as Proteus or Klippel-Trenaunay (K-T) syndromes, and for the therapeutic management of the different anomali …
Identification of the clinical and genetic characteristics of CLOVES syndrome is crucial for the differential diagnosis with o …
Vascular malformations syndromes: an update.
Martinez-Lopez A, Salvador-Rodriguez L, Montero-Vilchez T, Molina-Leyva A, Tercedor-Sanchez J, Arias-Santiago S. Martinez-Lopez A, et al. Curr Opin Pediatr. 2019 Dec;31(6):747-753. doi: 10.1097/MOP.0000000000000812. Curr Opin Pediatr. 2019. PMID: 31693582 Review.
PIK3CA-related overgrowth spectrum (PROS) is a group of rare genetic disorders with asymmetric overgrowth caused by somatic mosaic mutations in PI3K-AKT-mTOR pathway that encompass a heterogeneous group of rare disorder that are associated with the appearance of overgrowth. CL …
PIK3CA-related overgrowth spectrum (PROS) is a group of rare genetic disorders with asymmetric overgrowth caused by somatic mosaic mutations …
CLOVES Syndrome Diagnosis and Treatment in an Adult Patient.
Ferreira J, Gutiérrez JCL, Carneiro A, Araújo A, Sousa PP, Braga S, Simões JC, Carrilho C, Mesquita A. Ferreira J, et al. Ann Vasc Surg. 2021 Aug;75:533.e5-533.e9. doi: 10.1016/j.avsg.2021.03.044. Epub 2021 Apr 24. Ann Vasc Surg. 2021. PMID: 33905855
CLOVES syndrome is a rare, nonheritable sporadic overgrowth disorder. ...
CLOVES syndrome is a rare, nonheritable sporadic overgrowth disorder. ...
What is your diagnosis?
Panteliades M, Silva CM, Gontijo B. Panteliades M, et al. An Bras Dermatol. 2016 May-Jun;91(3):378-80. doi: 10.1590/abd1806-4841.20165897. An Bras Dermatol. 2016. PMID: 27438212 Free PMC article.
CLOVES syndrome is a rare, newly described, and relatively unknown syndrome, related to somatic mutations of the PIK3CA gene. ...
CLOVES syndrome is a rare, newly described, and relatively unknown syndrome, related to somatic mutations of the PIK3CA gene. …
Controversy on the management of patients carrying RET p.V804M mutation.
Alzahrani AS, Alswailem M, Alghamdi B, Rafiullah R, Aldawish M, Al-Hindi H. Alzahrani AS, et al. Endocrine. 2022 Feb;75(2):478-486. doi: 10.1007/s12020-021-02895-8. Epub 2021 Oct 12. Endocrine. 2022. PMID: 34637071 Review.
This variant was not found in DNA extracted from blood. This confirmed the diagnosis of CLOVES syndrome (Congenital Lipomatous Overgrowth, Vascular malformations, Epidermal nevi and Scoliosis, skeletal or spinal anomalies). ...
This variant was not found in DNA extracted from blood. This confirmed the diagnosis of CLOVES syndrome (Congenital Lipomatous …
Complex Truncal Masses in the Setting of CLOVES Syndrome: Aesthetic and Functional Implications.
Weissler JM, Shubinets V, Carney MJ, Low DW. Weissler JM, et al. Aesthetic Plast Surg. 2017 Jun;41(3):591-599. doi: 10.1007/s00266-016-0771-1. Epub 2016 Dec 28. Aesthetic Plast Surg. 2017. PMID: 28032156
METHODS: A single-institution retrospective review was performed for patients diagnosed with CLOVES syndrome. Patients undergoing excision of truncal vascular malformations were included. ...One patient with recurrence was subsequently treated with a combination of …
METHODS: A single-institution retrospective review was performed for patients diagnosed with CLOVES syndrome. Patients undergo …
Klippel-Trenaunay syndrome and spinal arteriovenous malformations: an erroneous association.
Alomari AI, Orbach DB, Mulliken JB, Bisdorff A, Fishman SJ, Norbash A, Alokaili R, Lord DJ, Burrows PE. Alomari AI, et al. AJNR Am J Neuroradiol. 2010 Oct;31(9):1608-12. doi: 10.3174/ajnr.A2167. Epub 2010 Jul 22. AJNR Am J Neuroradiol. 2010. PMID: 20651014 Free PMC article. Review.
Clinical data were either incompatible with the diagnosis of KTS or were inadequate to establish the diagnosis. Alternative possible diagnoses (CLOVES syndrome and CM-AVM) were suggested by the first author for 9 of the patients reported in these articles. ...
Clinical data were either incompatible with the diagnosis of KTS or were inadequate to establish the diagnosis. Alternative possible diagnos …
37 results