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Angiokeratoma

A vascular, horny neoplasm of the skin characterized by TELANGIECTASIS and secondary epithelial changes including acanthosis and hyperkeratosis.
Also Known As:
Angiokeratomas
Networked: 128 relevant articles (14 outcomes, 7 trials/studies)

Relationship Network

Disease Context: Research Results

Related Diseases

1. Fabry Disease (Fabry's Disease)
2. Hemangioma (Angioma)
3. Port-Wine Stain (Nevus Flammeus)
4. Vascular Malformations
5. Neurocutaneous Syndromes (Phakomatoses)

Experts

1. Cohen, Philip R: 5 articles (01/2021 - 03/2018)
2. Niu, Dau-Ming: 2 articles (10/2020 - 01/2018)
3. Schiffmann, Raphael: 2 articles (10/2020 - 07/2005)
4. Warnock, David G: 2 articles (10/2020 - 04/2020)
5. Baumgartner, Ján: 2 articles (12/2017 - 06/2016)
6. Šimaljaková, Mária: 2 articles (12/2017 - 06/2016)
7. Lin, Qiong-Zhu: 2 articles (01/2016 - 11/2014)
8. Zeng, Ying: 2 articles (01/2016 - 11/2014)
9. Zhan, Kui: 2 articles (01/2016 - 11/2014)
10. Hatfield, Jess: 1 article (01/2022)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Angiokeratoma:
1. ArgonIBA
2. Sirolimus (Rapamycin)FDA Link
3. Triamcinolone Acetonide (Azmacort)FDA LinkGeneric
4. EnzymesIBA
5. AntigensIBA
6. SialoglycoproteinsIBA
7. alpha-Galactosidase (Beano)IBA
8. GalactosidasesIBA
9. GlycosphingolipidsIBA
01/01/2009 - "Glycosphingolipid deposition in various tissues leads to episodic pain crises and acroparesthesias, gastrointestinal disturbances, angiokeratomas, corneal, and lenticular opacities, and eventually in the third to fifth decades of life, the kidney, heart and central nervous system are involved. "
01/01/2007 - "Fabry's disease is a congenital disorder of glycosphingolipid metabolism with an X-linked recessive inheritance, presenting with typical symptoms of pain crises, acroparesthesias, cutaneous and mucosal angiokeratomas, hypohidrosis, heart and kidney lesions, and other symptoms, which are described below. "
01/01/2002 - "Inability to prevent the progression of glycosphingolipid deposition causes significant morbidity (acroparesthesia, angiokeratoma, autonomic dysfunction, cardiomyopathy and deafness), and mortality from early onset strokes, heart attack and renal failure in adulthood. "
10/01/2008 - "Generalised systemic angiokeratoma constitute angiokeratoma corporis diffusum, a rare X-linked recessive inborn error of glycosphingolipid metabolism due to deficiency of alpha galactosidase A. "
01/01/2020 - "Fabry disease is an X-linked disorder of glycosphingolipid metabolism that results in progressive accumulation of neutral glycosphingolipids, predominantly globotriaosylsphingosine (Gb3) in lysosomes, as well as other cellular compartments of several tissues, causing multi-organ manifestations (acroparesthesias, hypohidrosis, angiokeratomas, signs and symptoms of cardiac, renal, cerebrovascular involvement). "
10. 3-hydroxy-5-estrane-17-carbonitrile (ACN)IBA

Therapies and Procedures

1. Lasers (Laser)
2. Solid-State Lasers
3. Dye Lasers
4. Therapeutics
5. Cryotherapy (Therapy, Cold)