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Disease Profile
Herpes zoster oticus
Prevalence estimates on Rare Medical Network websites are calculated based on data available from numerous sources, including US and European government statistics, the NIH, Orphanet, and published epidemiologic studies. Rare disease population data is recognized to be highly variable, and based on a wide variety of source data and methodologies, so the prevalence data on this site should be assumed to be estimated and cannot be considered to be absolutely correct.
Unknown
Age of onset
All ages
ICD-10
B02.2+ G53.0*
Inheritance
Autosomal dominant A pathogenic variant in only one gene copy in each cell is sufficient to cause an autosomal dominant disease.
Autosomal recessive Pathogenic variants in both copies of each gene of the chromosome are needed to cause an autosomal recessive disease and observe the mutant phenotype.
X-linked
dominant X-linked dominant inheritance, sometimes referred to as X-linked dominance, is a mode of genetic inheritance by which a dominant gene is carried on the X chromosome.
dominant X-linked dominant inheritance, sometimes referred to as X-linked dominance, is a mode of genetic inheritance by which a dominant gene is carried on the X chromosome.
X-linked
recessive Pathogenic variants in both copies of a gene on the X chromosome cause an X-linked recessive disorder.
recessive Pathogenic variants in both copies of a gene on the X chromosome cause an X-linked recessive disorder.
Mitochondrial or multigenic Mitochondrial genetic disorders can be caused by changes (mutations) in either the mitochondrial DNA or nuclear DNA that lead to dysfunction of the mitochondria and inadequate production of energy.
Multigenic or multifactor Inheritance involving many factors, of which at least one is genetic but none is of overwhelming importance, as in the causation of a disease by multiple genetic and environmental factors.
Not applicable
Other names (AKA)
Ramsay Hunt syndrome type 2 (formerly); Hunt's syndrome (formerly); Hunt syndrome (formerly);
Categories
Nervous System Diseases; Viral infections
Summary
Herpes zoster oticus is a common complication of shingles, an infection caused by the varicella-zoster
Treatment
FDA-Approved Treatments
The medication(s) listed below have been approved by the Food and Drug Administration (FDA) as orphan products for treatment of this condition. Learn more orphan products.
- Capsaicin (Brand name: Qutenza) Manufactured by NeurogesX, Inc.
FDA-approved indication: Management of neuropathic pain associated with postherpetic neuralgia
National Library of Medicine Drug Information Portal
Organizations
Support and advocacy groups can help you connect with other patients and families, and they can provide valuable services. Many develop patient-centered information and are the driving force behind research for better treatments and possible cures. They can direct you to research, resources, and services. Many organizations also have experts who serve as medical advisors or provide lists of doctors/clinics. Visit the group’s website or contact them to learn about the services they offer. Inclusion on this list is not an endorsement by GARD.
Organizations Supporting this Disease
-
National Shingles Foundation
603 West 115 St. Suite 371
New York, NY 10025
Telephone: 212-222-3390
Fax: 212-222-8627
E-mail: [email protected]
Website: https://www.vzvfoundation.org/
Learn more
These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.
Where to Start
- MayoClinic.com provides information about Ramsay Hunt syndrome. Click on the above link to access this information.
- MedlinePlus was designed by the National Library of Medicine to help you research your health questions, and it provides more information about this topic.
- The Merck Manuals Online Medical Library provides information on this condition for patients and caregivers.
- The National Institute of Neurological Disorders and Stroke (NINDS) collects and disseminates research information related to neurological disorders. Click on the link to view information on this topic.
- The National Organization for Rare Disorders (NORD) has a report for patients and families about this condition. NORD is a patient advocacy organization for individuals with rare diseases and the organizations that serve them.
In-Depth Information
- Medscape Reference provides information on this topic. You may need to register to view the medical textbook, but registration is free.
Ramsay Hunt Syndrome
Herpes Zoster Oticus - The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. Monarch’s tools are designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health. Visit the website to explore the biology of this condition.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Herpes zoster oticus. Click on the link to view a sample search on this topic.
References
- NINDS Herpes Zoster Oticus Information Page. National Institute of Neurological Disorders and Stroke. February 14, 2011; https://www.ninds.nih.gov/disorders/ramsay2/ramsay2.htm.
- Daniel Kim. Ramsay Hunt Syndrome. National Organization for Rare Disorders (NORD). 2011; https://rarediseases.org/rare-diseases/ramsay-hunt-syndrome/.
- Ramsay Hunt Syndrome. Mayo Clinic. January 2, 2014; https://www.mayoclinic.org/diseases-conditions/ramsay-hunt-syndrome/basics/treatment/con-20029560?METHOD=print&p=1.
- Joseph V. Campellone. Ramsay Hunt syndrome. MedlinePlus. May 28, 2014; https://www.nlm.nih.gov/medlineplus/ency/article/001647.htm.
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