Just diagnosed with Pudendal neuralgia?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Pudendal neuralgia, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Pudendal neuralgia hub →Overview
Pudendal neuralgia is a rare condition. Also known as Alcock syndrome, Pudendal algia, Pudendal neuralgia, Pudendal neuralgia by pudendal nerve entrapment, Pudendal neuropathic pain syndrome, Pudendal neuropathy, Pudendalgia. Tomeko brings together the specialists, research, clinical trials, treatments and community for Pudendal neuralgia so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:60039 · ICD-10 G58.8 · GARD 0010713
Find care for Pudendal neuralgia
Authoritative references for Pudendal neuralgia
Research & market landscape for Pudendal neuralgia
Following Pudendal neuralgia for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Pudendal neuralgia — the real-world landscape behind the condition, in one place.
- Latest Pudendal neuralgia research on PubMed ↗
- Recruiting Pudendal neuralgia trials on ClinicalTrials.gov ↗
- Explore the Pudendal neuralgia research & specialist footprint on Tomeko
Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for Pudendal neuralgia and every rare condition. See how Tomeko works with industry →
Common questions
What is Pudendal neuralgia?
Pudendal neuralgia is a rare condition. Also known as Alcock syndrome, Pudendal algia, Pudendal neuralgia, Pudendal neuralgia by pudendal nerve entrapment, Pudendal neuropathic pain syndrome, Pudendal neuropathy, Pudendalgia. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Pudendal neuralgia together in one place.
What are the symptoms of Pudendal neuralgia?
Symptoms of Pudendal neuralgia vary from person to person. For a reviewed, plain-language overview see the authoritative references below (NIH GARD, Orphanet), and discuss your own symptoms with a clinician who treats Pudendal neuralgia.
How is Pudendal neuralgia treated?
Treatment for Pudendal neuralgia depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Pudendal neuralgia, and review current options with them.
What causes Pudendal neuralgia — is it genetic?
The cause and inheritance of Pudendal neuralgia are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Pudendal neuralgia can explain what it means for you and your family.
I was just diagnosed with Pudendal neuralgia — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Pudendal neuralgia, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Pudendal neuralgia?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Pudendal neuralgia, filtered to your area.
Are there clinical trials for Pudendal neuralgia?
Tomeko shows live, recruiting studies for Pudendal neuralgia from ClinicalTrials.gov on the hub.
Related conditions
Other conditions on Tomeko you may be looking for:
- Acetazolamide-responsive myotonia
- Acquired porencephaly
- Actin accumulation myopathy
- Action myoclonus-renal failure syndrome
- Acute disseminated encephalomyelitis
- Acute disseminated encephalomyelitis with anti-MOG antibodies
- Acute disseminated encephalomyelitis without anti-MOG antibodies
- Acute encephalopathy with biphasic seizures and late reduced diffusion