Weber syndrome

Common Name(s)

Weber syndrome

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Weber syndrome" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Weber syndrome" returned 191 free, full-text research articles on human participants. First 3 results:

Sturge-Weber Syndrome.
 

Author(s): Shivang Desai, Charles Glasier

Journal: N. Engl. J. Med.. 2017 Aug;377(9):e11.

 

Last Updated: 30 Aug 2017

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Hereditary hemorrhagic telangiectasia, liver disease and elevated serum testosterone (Osler-Weber-Rendu syndrome): a case report.
 

Author(s): R Dissanayake, K P K Y M D S Wickramarathne, S N Seneviratne, S N Perera, M U J Fernando, V P Wickramasinghe

Journal:

 

A Sri Lankan girl with hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome) is described.

Last Updated: 24 Jan 2017

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Growing skull hemangioma: first and unique description in a patient with Klippel-Trénaunay-Weber syndrome.
 

Author(s): Lars E van der Loo, Jan Beckervordersandforth, Albert J Colon, Olaf E M G Schijns

Journal: Acta Neurochir (Wien). 2017 Feb;159(2):397-400.

 

We present the first and unique case of a rapid-growing skull hemangioma in a patient with Klippel-Trénaunay-Weber syndrome. This case report provides evidence that not all rapid-growing, osteolytic skull lesions need to have a malignant character but certainly need a histopathological ...

Last Updated: 8 Nov 2016

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Weber syndrome" returned 12 free, full-text review articles on human participants. First 3 results:

Current Therapeutic Options in Sturge-Weber Syndrome.
 

Author(s): Anne Comi

Journal: Semin Pediatr Neurol. 2015 Dec;22(4):295-301.

 

Sturge-Weber syndrome is a vascular malformation syndrome consisting of a facial port-wine birthmark associated with malformed leptomeningeal blood vessels and a choroid "angioma" of the eye. It is a rare neurocutaneous disorder that occurs sporadically, is not inherited, and is caused ...

Last Updated: 26 Dec 2015

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Ophthalmic Alterations in the Sturge-Weber Syndrome, Klippel-Trenaunay Syndrome, and the Phakomatosis Pigmentovascularis: An Independent Group of Conditions?
 

Author(s): Solmaz Abdolrahimzadeh, Vittorio Scavella, Lorenzo Felli, Filippo Cruciani, Maria Teresa Contestabile, Santi Maria Recupero

Journal: Biomed Res Int. 2015 ;2015():786519.

 

The phakomatoses have been traditionally defined as a group of hereditary diseases with variable expressivity characterized by multisystem tumors with possible malignant transformation. The Sturge-Weber syndrome, Klippel-Trenaunay syndrome, and the phakomatosis pigmentovascularis ...

Last Updated: 9 Oct 2015

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Image diagnosis: Weber syndrome: a rare presentation of acute leukemia-a case report and review of the literature.
 

Author(s): Valliappan Muthu, Santosh Kumar, Gaurav Prakash, Prashant Sharma, Subhash Varma

Journal: Perm J. 2015 ;19(1):83-5.

 

Last Updated: 9 Feb 2015

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Innovative Approaches to Gauge Progression of Sturge-Weber Syndrome
 

Status: Recruiting

Condition Summary: Sturge-Weber Syndrome

 

Last Updated: 11 Sep 2017

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Trial of Sirolimus for Cognitive Impairment in Sturge-Weber Syndrome
 

Status: Recruiting

Condition Summary: Sturge-Weber Syndrome

 

Last Updated: 11 Sep 2017

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Treatment of Port-wine Mark in Sturge-Weber Syndrome Using Topical Timolol
 

Status: Recruiting

Condition Summary: Sturge Weber Syndrome; Port-wine Mark

 

Last Updated: 12 May 2017

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