Glomuvenous malformations

Common Name(s)

Glomuvenous malformations

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Glomuvenous malformations" 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 "Glomuvenous malformations" returned 6 free, full-text research articles on human participants. First 3 results:

Somatic uniparental isodisomy explains multifocality of glomuvenous malformations.
 

Author(s): Mustapha Amyere, Virginie Aerts, Pascal Brouillard, Brendan A S McIntyre, François P Duhoux, Michel Wassef, Odile Enjolras, John B Mulliken, Olivier Devuyst, Hélène Antoine-Poirel, Laurence M Boon, Miikka Vikkula

Journal: Am. J. Hum. Genet.. 2013 Feb;92(2):188-96.

 

Inherited vascular malformations are commonly autosomal dominantly inherited with high, but incomplete, penetrance; they often present as multiple lesions. We hypothesized that Knudson's two-hit model could explain this multifocality and partial penetrance. We performed a systematic ...

Last Updated: 11 Feb 2013

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Multiple disseminated glomuvenous malformations: do we know enough?
 

Author(s): C Solovan, Elena Chiticariu, Doina Beinsan, Sabina Zurac, Flavia Baderca

Journal: Rom J Morphol Embryol. 2012 ;53(4):1077-80.

 

Multiple glomuvenous malformations (GVMs), also known as glomangiomas, are uncommon entities with histological features of both glomus cells proliferation and venous malformation. A 14-year-old boy was admitted to our clinic with multiple dermal blue nodules, disseminated in different ...

Last Updated: 10 Jan 2013

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Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation.
 

Author(s): Matthew G Butler, Susan L Dagenais, José L Garcia-Perez, Pascal Brouillard, Miikka Vikkula, Peter Strouse, Jeffrey W Innis, Thomas W Glover

Journal: Am. J. Med. Genet. A. 2012 Apr;158A(4):839-49.

 

Two hereditary syndromes, lymphedema-distichiasis (LD) syndrome and blepharo-chelio-dontic (BCD) syndrome include the aberrant growth of eyelashes from the meibomian glands, known as distichiasis. LD is an autosomal dominant syndrome primarily characterized by distichiasis and the ...

Last Updated: 27 Mar 2012

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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 "Glomuvenous malformations" returned 1 free, full-text review articles on human participants. First 3 results:

Glomuvenous Malformations (Familial generalized multiple glomangiomas).
 

Author(s): Jeremy A Brauer, Robert Anolik, Julia Tzu, Shane Meehan, Colette D Lieber, Roy G Geronemus

Journal:

 

A 15-year-old boy with a diagnosis of generalized multiple glomangiomas was referred for evaluation and treatment of enlarging and increasingly painful lesions on his right ankle. The patient underwent a series of two treatments with long-pulsed KTP 1064 nm laser that resulted in ...

Last Updated: 27 Oct 2011

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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.