National Center for Advancing and Translational Sciences Genetic and Rare Diseases Information Center, a program of the National Center for Advancing and Translational Sciences

Multifocal lymphangioendotheliomatosis with thrombocytopenia


Other Names:
MLT; Cutaneovisceral angiomatosis-thrombocytopenia syndrome; Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome; MLT; Cutaneovisceral angiomatosis-thrombocytopenia syndrome; Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome; cutaneovisceral angiomatosis with thrombocytopenia See More
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Research helps us better understand diseases and can lead to advances in diagnosis and treatment. This section provides resources to help you learn about medical research and ways to get involved.

Clinical Research Resources

  • ClinicalTrials.gov lists trials that are related to Multifocal lymphangioendotheliomatosis with thrombocytopenia. Click on the link to go to ClinicalTrials.gov to read descriptions of these studies.

    Please note: Studies listed on the ClinicalTrials.gov website are listed for informational purposes only; being listed does not reflect an endorsement by GARD or the NIH. We strongly recommend that you talk with a trusted healthcare provider before choosing to participate in any clinical study.

Patient Registry

  • The Registry for Vascular Anomalies Associated With Coagulopathy aims to learn more about multifocal lymphangioendotheliomatosis with thrombocytopenia (MLT). This study is collecting detailed clinical data on the distribution of disease, disease severity, and complications. This data will be used to create diagnostic criteria and an evaluation protocol for infants with this disease.

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

Social Networking Websites

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

In-Depth Information

  • 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 Multifocal lymphangioendotheliomatosis with thrombocytopenia. Click on the link to view a sample search on this topic.

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