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About 543 results

ALLMedicine™ Klippel-Trenaunay Syndrome Center

Research & Reviews  259 results

Hidradenitis suppurativa associated with a novel NCSTN mutation and concomitant Klippel...
https://doi.org/10.1684/ejd.2021.4005
European Journal of Dermatology : EJD; Lin YY, Lin LH et. al.

Apr 5th, 2021 - Hidradenitis suppurativa associated with a novel NCSTN mutation and concomitant Klippel-Trenaunay syndrome.|2021|Lin YY,Lin LH,Kang J,Li CR,Xiao XM,|

Klippel-Trenaunay syndrome in a young patient with the involvement of gastrointestinal ...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7929800
BMJ Case Reports; Shaikh OH, Kumbhar US et. al.

Mar 3rd, 2021 - Klippel-Trenaunay syndrome (KTS) is a rare congenital disorder characterised by capillary and venous malformations and soft-tissue hypertrophy with or without lymphatic malformation. The involvement of the gastrointestinal tract and genitourinary ...

Case Series of Concomitant Klippel-Trenaunay Syndrome and May-Thurner Syndrome.
https://doi.org/10.1177/1538574421995011
Vascular and Endovascular Surgery; Charitable JF, Yilmaz O et. al.

Feb 18th, 2021 - Klippel-Trenaunay syndrome is a rare vascular disorder which includes leg swelling, or lower extremity deep venous reflux/thrombosis as a presenting symptom. May-Thurner syndrome is also a rare pathology involving compression of the left common il...

Klippel-Trenaunay syndrome associated to squamous cell carcinoma: a safe choice.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7875257
BMJ Case Reports; Mattioli M, Pagliariccio G et. al.

Feb 10th, 2021 - Klippel-Trenaunay syndrome associated to squamous cell carcinoma: a safe choice.|2021|Mattioli M,Pagliariccio G,Carbonari L,|

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Clinicaltrials.gov  273 results

Hidradenitis suppurativa associated with a novel NCSTN mutation and concomitant Klippel...
https://doi.org/10.1684/ejd.2021.4005
European Journal of Dermatology : EJD; Lin YY, Lin LH et. al.

Apr 5th, 2021 - Hidradenitis suppurativa associated with a novel NCSTN mutation and concomitant Klippel-Trenaunay syndrome.|2021|Lin YY,Lin LH,Kang J,Li CR,Xiao XM,|

Klippel-Trenaunay syndrome in a young patient with the involvement of gastrointestinal ...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7929800
BMJ Case Reports; Shaikh OH, Kumbhar US et. al.

Mar 3rd, 2021 - Klippel-Trenaunay syndrome (KTS) is a rare congenital disorder characterised by capillary and venous malformations and soft-tissue hypertrophy with or without lymphatic malformation. The involvement of the gastrointestinal tract and genitourinary ...

Case Series of Concomitant Klippel-Trenaunay Syndrome and May-Thurner Syndrome.
https://doi.org/10.1177/1538574421995011
Vascular and Endovascular Surgery; Charitable JF, Yilmaz O et. al.

Feb 18th, 2021 - Klippel-Trenaunay syndrome is a rare vascular disorder which includes leg swelling, or lower extremity deep venous reflux/thrombosis as a presenting symptom. May-Thurner syndrome is also a rare pathology involving compression of the left common il...

Klippel-Trenaunay syndrome associated to squamous cell carcinoma: a safe choice.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7875257
BMJ Case Reports; Mattioli M, Pagliariccio G et. al.

Feb 10th, 2021 - Klippel-Trenaunay syndrome associated to squamous cell carcinoma: a safe choice.|2021|Mattioli M,Pagliariccio G,Carbonari L,|

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News  2 results

International Sturge-Weber Research Network Is Launched
https://www.mdedge.com/neurology/article/105112/rare-diseases/international-sturge-weber-research-network-launched

Dec 11th, 2015 - The Sturge-Weber Foundation has announced the formation of the SWF International Research Network, an initiative to support international collaboration among medical experts and scientific researchers in the treatment of Sturge-Weber syndrome, por.

Limb Hyperplasia: Case Report of an Unusual Variant of Klippel-Trenaunay Syndrome and Review of the Literature
https://www.mdedge.com/dermatology/article/67826/limb-hyperplasia-case-report-unusual-variant-klippel-trenaunay-syndrome
Gober-Wilcox JK, Gardner DL et. al.

Klippel-Trenaunay syndrome (KTS) is a rare disorder involving a triad of cutaneous capillary malformations (port-wine stain), varicose veins or venous malformations, and bony or soft tissue hyperplasia of an extremity. It is one of many heterogene.

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Patient Education  9 results see all →