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 184 free, full-text research articles on human participants. First 3 results:

Analysis of Epileptic Discharges from Implanted Subdural Electrodes in Patients with Sturge-Weber Syndrome.
 

Author(s): Yasushi Iimura, Hidenori Sugano, Madoka Nakajima, Takuma Higo, Hiroharu Suzuki, Hajime Nakanishi, Hajime Arai

Journal:

 

Almost two-thirds of patients with Sturge-Weber syndrome (SWS) have epilepsy, and half of them require surgery for it. However, it is well known that scalp electroencephalography (EEG) does not demonstrate unequivocal epileptic discharges in patients with SWS. Therefore, we analyzed ...

Last Updated: 8 Apr 2016

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Klippel-Trenaunay-Weber Syndrome with Kasabach-Merritt Coagulopathy and Hydronephrosis.
 

Author(s): Lata Bhat, Supriya Bisht, Kavita Khanijo

Journal: Indian Pediatr. 2015 Nov;52(11):987-8.

 

Klippel-Trenaunay-Weber Syndrome is a rare syndrome, consisting of vascular malformation of blood and lymph vessels.

Last Updated: 30 Nov 2015

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Phakomatosis pigmentovascularis Type IIb, Sturge-Weber syndrome and cone shaped tongue: An unusual association.
 

Author(s): Swetalina Pradhan, Satyadarshi Patnaik, Tanmay Padhi, Bibhu Prasad Nayak

Journal: Indian J Dermatol Venereol Leprol. ;81(6):614-6.

 

Last Updated: 30 Oct 2015

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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 11 free, full-text review articles on human participants. First 3 results:

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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Transition into adulthood: tuberous sclerosis complex, Sturge-Weber syndrome, and Rasmussen encephalitis.
 

Author(s): Elizabeth A Thiele, Tiziana Granata, Sara Matricardi, Harry T Chugani

Journal: Epilepsia. 2014 Aug;55 Suppl 3():29-33.

 

Children with tuberous sclerosis complex, Sturge-Weber syndrome, and Rasmussen encephalitis all have complex but differing needs in the process of transition/transfer to adult care. All three may be associated with long-term normal intelligence or a varying degree of intellectual ...

Last Updated: 11 Sep 2014

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Symptoms, Diagnosis, and Treatment

There are currently no related results available in Genetics Home Reference.

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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: 12 Oct 2015

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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: 18 Dec 2015

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Lymphatic Anomalies Registry
 

Status: Recruiting

Condition Summary: Lymphatic Malformation; Generalized Lymphatic Anomaly (GLA); Central Conducting Lymphatic Anomaly; CLOVES Syndrome; Gorham-Stout Disease ("Disappearing Bone Disease"); Blue Rubber Bleb Nevus Syndrome; Kaposiform Lymphangiomatosis; Kaposiform Hemangioendothelioma/Tufted Angioma; Klippel-Trenaunay Syndrome; Lymphangiomatosis

 

Last Updated: 26 Jul 2016

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