Characterization of a distinct syndrome that associates complex truncal overgrowth, vascular, and acral anomalies: a descriptive study of 18 cases of CLOVES syndrome.
about
Somatic mosaic activating mutations in PIK3CA cause CLOVES syndromeNeurocutaneous Manifestations of Genetic MosaicismPIK3CA-related overgrowth spectrum (PROS): diagnostic and testing eligibility criteria, differential diagnosis, and evaluationLymphatic and other vascular malformative/overgrowth disorders are caused by somatic mutations in PIK3CAVascular anomalies: A pictorial review of nomenclature, diagnosis and treatmentExtensive Fetal Congenital Subcutaneous Mixed Venous Lymphatic Lesion: Prenatal Diagnosis and Postnatal Management.PIK3CA-associated developmental disorders exhibit distinct classes of mutations with variable expression and tissue distribution.Klippel-Trenaunay syndrome and spinal arteriovenous malformations: an erroneous association.Overlapping biomarkers, pathways, processes and syndromes in lymphatic development, growth and neoplasia.Complex vascular anomalies.Diffuse capillary malformation in association with fetal pleural effusion: report of five patients.Approach to the Diagnosis of Overgrowth Syndromes.Complex Truncal Masses in the Setting of CLOVES Syndrome: Aesthetic and Functional Implications.CLOVES syndrome: review of a PIK3CA-related overgrowth spectrum (PROS).Vascular Stains: Proposal for a Clinical Classification to Improve Diagnosis and Management.PI3K Signaling in Tissue Hyper-Proliferation: From Overgrowth Syndromes to Kidney Cysts.Sonographic screening for Wilms tumor in children with CLOVES syndrome.The effect of rapamycin, NVP-BEZ235, aspirin, and metformin on PI3K/AKT/mTOR signaling pathway of PIK3CA-related overgrowth spectrum (PROS).A rare newly described overgrowth syndrome with vascular malformations-Cloves syndrome.CLOVES Syndrome: Severe Neonatal Presentation.Another epidermal naevus with polyostotic anomalies?A Neonate with CLOVES Syndrome.Lethal outcomes in Klippel-Trenaunay syndrome.Causal somatic mutations in urine DNA from persons with the CLOVES subgroup of the PIK3CA Related Overgrowth Spectrum (PROS).Utilizing lymphatic cell markers to visualize human lymphatic abnormalities.Mosaic disorders and the Taxonomy of Human Disease.Assessment of PTEN-associated vascular malformations in a patient with Bannayan-Riley-Ruvalcaba syndrome.Capillary-venous malformation in the upper limb.Prenatal diagnosis of CLOVES syndrome confirmed by detection of a mosaic PIK3CA mutation in cultured amniocytes.Clinical delineation and natural history of the PIK3CA-related overgrowth spectrum.
P2860
Q24608709-81AD4577-2047-464B-B408-7AE75C3C4599Q28070020-98CDCBAD-58E4-49FB-873D-77E10CAAF7EFQ28081443-19E2843C-B59E-4B90-A065-EC9955C96635Q28256964-E054BEC5-54CB-4F07-9D52-DA0103BD2126Q34251804-E8B5F894-89A4-4600-963D-09B166D16035Q35852689-30C8367C-C628-4E60-B693-D21C26D21AF4Q37248504-69713A72-37FF-44B3-92DE-8D39A5415A80Q37774790-7751E302-60B3-4845-B40C-D9D9A3AE0EACQ38026529-B813B0DE-942D-436B-B761-8E7E96376FDCQ38132619-44FA4400-5624-4877-961F-A6361FB2A5E8Q38341338-5905A3FD-1C1E-4F07-83A5-B64731730CBBQ38672998-870F837B-2A92-40E9-8B9C-5E1B37692949Q38776746-0054B07F-EB88-4D4D-8B68-198219F28EAEQ38899877-042D786A-A4AA-433C-8595-211AA6FCEB7CQ38908005-D4DBDE86-28CF-4285-8C32-2EF5164960ECQ39206695-F7493C26-3829-47E6-97A7-B5241ADBF6D1Q39382026-70110DE6-25B5-43B8-B1F6-796D59ECD61CQ41233466-9E502A66-AA04-4995-B303-422160A2EBFEQ42058207-FC670B1C-9187-4FE7-B497-1A4A5A30EEADQ42128212-2A61835E-5BEC-4C17-915C-7CA9F3078B81Q42606935-075B279E-2DFA-422D-89A9-4947022E15FBQ42978050-22DE11B2-2488-4445-8FDE-2FD8770579C8Q45927410-6E7254C0-D740-4E37-9180-0067A755AC1AQ47221823-FA988DD1-B118-4796-86BB-48A30F6391ABQ48133682-6521AB49-443B-4D4E-962C-0BE7E0364F44Q48508191-DBDFA149-DE0F-456F-A3E9-68A82AAF8DA9Q51673156-E06E3539-7EC6-4EF1-A941-82AC333CB034Q53653263-EE5021C8-0489-4574-BB17-24DC13307BC0Q54336308-140C54F9-EC5E-4ED5-85DB-F75A99CFAA06Q54356163-9610AAC1-F265-455E-837B-2A5A388B4CB0
P2860
Characterization of a distinct syndrome that associates complex truncal overgrowth, vascular, and acral anomalies: a descriptive study of 18 cases of CLOVES syndrome.
description
2009 nî lūn-bûn
@nan
2009 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Characterization of a distinct ...... f 18 cases of CLOVES syndrome.
@ast
Characterization of a distinct ...... f 18 cases of CLOVES syndrome.
@en
type
label
Characterization of a distinct ...... f 18 cases of CLOVES syndrome.
@ast
Characterization of a distinct ...... f 18 cases of CLOVES syndrome.
@en
prefLabel
Characterization of a distinct ...... f 18 cases of CLOVES syndrome.
@ast
Characterization of a distinct ...... f 18 cases of CLOVES syndrome.
@en
P1476
Characterization of a distinct ...... f 18 cases of CLOVES syndrome.
@en
P356
10.1097/MCD.0B013E328317A716
P577
2009-01-01T00:00:00Z