Overview
Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome, sometimes called WILD syndrome, is a very rare inherited condition that affects several parts of the body at once. The name describes its four main features: stubborn warts that keep coming back, a weakened immune system, swelling in the limbs caused by poor lymph fluid drainage (lymphedema), and abnormal tissue changes in the genital and anal area (anogenital dysplasia). These features can appear together or in different combinations depending on the person. The weakened immune system means the body has trouble fighting off certain infections, especially viruses like human papillomavirus (HPV), which causes the persistent warts. The lymphedema usually affects the legs and can cause significant swelling and discomfort. The anogenital dysplasia refers to abnormal cell changes in the skin around the genitals and anus, which may need close monitoring because of a potential risk of developing into cancer over time. Treatment focuses on managing each symptom separately. There is currently no cure. Doctors work to control warts, treat infections, manage swelling with compression garments and physical therapy, and monitor the anogenital area closely. A team of specialists is usually needed to provide the best care.
Also known as:
Key symptoms:
Persistent, recurring warts on the skinWeakened immune system making infections harder to fightSwelling in the legs or arms due to poor lymph drainage (lymphedema)Abnormal tissue changes around the genitals and anus (anogenital dysplasia)Frequent or unusual infectionsSkin changes or lesions in the anogenital areaDifficulty fighting off HPV (the virus that causes warts)Heaviness or tightness in swollen limbs
Autosomal dominant
Passed on from just one parent; each child has about a 50% chance of inheriting it
Variable
Can begin at different ages, from infancy through adulthood
FDA & Trial Timeline
1 eventSorlandet Hospital HF — NA
Data sourced from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.
Treatments
No FDA-approved treatments are currently listed for Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome.
View clinical trials →Clinical Trials
View all trials with filters →No actively recruiting trials found for Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome at this time.
New trials open frequently. Follow this disease to get notified.
Specialists
View all specialists →No specialists are currently listed for Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome.
Treatment Centers
8 centersBaylor College of Medicine Rare Disease Center ↗
Baylor College of Medicine
📍 Houston, TX
🏥 NORDStanford Medicine Rare Disease Center ↗
Stanford Medicine
📍 Stanford, CA
🔬 UDNNIH Clinical Center Undiagnosed Diseases Program ↗
National Institutes of Health
📍 Bethesda, MD
🔬 UDNUCLA UDN Clinical Site ↗
UCLA Health
📍 Los Angeles, CA
🔬 UDNBaylor College of Medicine UDN Clinical Site ↗
Baylor College of Medicine
📍 Houston, TX
🔬 UDNHarvard/MGH UDN Clinical Site ↗
Massachusetts General Hospital
📍 Boston, MA
🏥 NORDMayo Clinic Center for Individualized Medicine ↗
Mayo Clinic
📍 Rochester, MN
👤 Mayo Clinic Center for Individualized Medicine
🏥 NORDUCLA Rare Disease Day Program ↗
UCLA Health
📍 Los Angeles, CA
Travel Grants
No travel grants are currently matched to Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome.
Community
No community posts yet. Be the first to share your experience with Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome.
Start the conversation →Latest news about Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome
Disease timeline:
New recruiting trial: Where Wild Things Grow: Nature- and Activity-based Group Interventions for Neurodivergent Children and Youth
A new clinical trial is recruiting patients for Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome
Caregiver Resources
NORD Caregiver Resources
Support, advocacy, and financial assistance for caregivers of rare disease patients.
Mental Health Support
Rare disease caregiving can be isolating. Connect with counseling and peer support.
Family & Caregiver Grants
Financial assistance programs specifically for caregivers of rare disease patients.
Social Security Disability
Learn how rare disease patients may qualify for SSDI/SSI benefits.
Questions for your doctor
Bring these to your next appointment
- Q1.Which specialists should be part of my care team, and how often should I see each one?,What genetic testing should I have, and should my family members be tested too?,How should I monitor the anogenital area for cancer risk, and how often?,What is the best way to manage my lymphedema day to day?,Are there any clinical trials or research studies I could join?,What infections should I watch out for, and when should I go to the emergency room?,Are there patient support groups or rare disease networks that could help me connect with others who have this condition?
Common questions about Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome
What is Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome?
Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome, sometimes called WILD syndrome, is a very rare inherited condition that affects several parts of the body at once. The name describes its four main features: stubborn warts that keep coming back, a weakened immune system, swelling in the limbs caused by poor lymph fluid drainage (lymphedema), and abnormal tissue changes in the genital and anal area (anogenital dysplasia). These features can appear together or in different combinations depending on the person. The weakened immune system means the body has trouble fighting off cer
How is Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome inherited?
Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome follows a autosomal dominant inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.