Other Names for this Disease
- 17p11.2 microduplication syndrome
- Duplication 17p11.2 syndrome
- Potocki-Lupski syndrome (dup(17)(p11.2p11.2))
- Trisomy 17p11.2
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- About Potocki-Lupski (dup17p11.2) Syndrome. Baylor College of Medicine. October 4, 2013; https://www.bcm.edu/departments/molecular-and-human-genetics/potocki_lupski/index.cfm?PMID=10619. Accessed 1/22/2014.
- Frequently Asked Questions (FAQs). Baylor College of Medicine. May 3, 2013; https://www.bcm.edu/departments/molecular-and-human-genetics/potocki_lupski/index.cfm?PMID=10628. Accessed 1/22/2014.
Your Questions Answeredby the Genetic and Rare Diseases Information Center
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- Baylor College of Medicine has developed a website on Potocki-Lupski syndrome. This website is intended to provide information to patients, families, and physicians and to develop a support network for those coping with this condition.
- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- 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 Potocki-Lupski syndrome. Click on the link to view a sample search on this topic.