Finding useful health information on the Internet can be difficult, but we’re here to help. This page gathers quality information from trusted sources. You can learn more about the disease, visit handpicked websites, and find resources to help you in your daily life. Need more information? Click the menu on the left to find more!
CLOSE
Medical Disclaimer
The medical information on this site is provided as an information resource only, and is not to be used or relied on for any diagnostic or treatment purposes. This information is not intended to be patient education, does not create any patient-physician relationship, and should not be used as a substitute for professional diagnosis and treatment.
Cutaneous larva migrans
Overview
Cutaneous larva migrans (CLM) is a skin infection caused by various parasites from the hookworm family (ancylostomatidae). These parasites are usually found in tropical and sub-tropical areas and live in animal hosts such as dogs, cats, and wild animals. It is most commonly contracted by coming into contact with the contaminated animal feces, usually on the ground. Though in animals this infection can spread into deeper tissues, in humans, the larva can only penetrate the upper layer of skin. Symptoms include very itchy red skin patches in the affected area that look like worm-like burrows. The skin patches may be painful and excessive scratching may cause secondary bacterial infections. CLM will usually go away on its own in a couple of weeks to months, but the process can be facilitated using certain topical or oral drugs. Anti-itch creams such as cortisone or Benadryl can help with symptom relief. To help prevent contracting this infection, wear shoes when walking in soil and beaches in tropical/sub-tropical areas. If you or a family member has contracted CLM, talk with your doctor about the most current treatment options.
Trusted Medical Sites
Genetic & Rare Diseases Information Center (GARD)
GARD provides the public with access to current, reliable, and easy-to-understand information about rare or genetic diseases in English or Spanish.
Support Organizations
Support organizations can provide help and guidance in areas such as peer matching, education and training, and therapy and counseling.
Disease Resources
Resources can help guide your quest for factual and reliable information.
Displaying 1-4 of 4 results.
The Progeria Handbook; A Guide for Families and Health Care Providers of Children with Progeria.
This 100-page handbook helps answer many questions for children with Progeria about how to optimize quality of life through daily care and medical treatment. Contains basic health facts,daily care recommendations and extensive treatment guidelines.
AAMDSIF Online Academy (webinars)
200+ FREE webinars for patients, families and caregivers about rare blood cancers and bone marrow failure diseases.
Educational Resources
Publications, links to patient conferences and webinars
Disease Information
Descriptions of various rare blood cancers and bone marrow failure diseases.