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SUNCT Syndrome

A primary headache disorder that is characterized by frequent short-lasting, unilateral, neuralgiform pain attacks in the ocular area, with CONJUNCTIVA fluid-filling and tearing. SUNCT syndrome is usually resistant to treatment.
Also Known As:
SUNCT Syndromes; Syndrome, SUNCT; Syndromes, SUNCT
Networked: 56 relevant articles (6 outcomes, 3 trials/studies)

Relationship Network

Disease Context: Research Results

Related Diseases

1. Headache (Headaches)
2. Headache Disorders (Headache Syndromes)
3. Prescription Drug Overuse
4. Prolactinoma (Prolactinomas)
5. Pain (Aches)

Experts

1. Goadsby, P J: 3 articles (10/2006 - 04/2002)
2. Matharu, M S: 2 articles (11/2004 - 04/2002)
3. Nappi, G: 2 articles (12/2003 - 11/2001)
4. El Amrani, M: 2 articles (06/2002 - 01/2000)
5. Benito-Leon, J: 2 articles (06/2002 - 04/2002)
6. Berbel, A: 2 articles (06/2002 - 04/2002)
7. Martinez-Salio, A: 2 articles (06/2002 - 04/2002)
8. Porta-Etessam, J: 2 articles (06/2002 - 04/2002)
9. Kawabata, Kazune: 1 article (03/2021)
10. Sago, Teppei: 1 article (03/2021)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to SUNCT Syndrome:
1. Lamotrigine (Lamictal)FDA LinkGeneric
2. Gabapentin (Neurontin)FDA LinkGeneric
3. Lidocaine (Xylocaine)FDA LinkGeneric
4. GlucocorticoidsIBA
5. Anesthetics (Anesthetic Agents)IBA
6. Topiramate (Topamax)FDA LinkGeneric
7. Oxcarbazepine (Trileptal)FDA LinkGeneric
8. Therapeutic UsesIBA
9. Type A Botulinum Toxins (Botox)FDA Link
10. Dopamine Agonists (Dopamine Agonist)IBA

Therapies and Procedures

1. Surgical Decompression
2. Therapeutics
3. Drug Therapy (Chemotherapy)
4. Intravenous Administration
5. Deep Brain Stimulation