Other Names for this Disease
- Tetra-amelia, autosomal recessive
- Tetraamelia, autosomal recessive
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mutation in the WNT3 gene in one family, and it appears to be inherited in an autosomal recessive manner.Tetra-amelia syndrome is a very rare disorder characterized by the absence of all four limbs. This syndrome can also cause severe malformations of other parts of the body, including the face and head, heart, nervous system, skeleton, and genitalia. The lungs are underdeveloped in many cases, which makes breathing difficult or impossible. Because children with tetra-amelia syndrome have such serious medical problems, most are stillborn or die shortly after birth. The condition has been associated with a
Last updated: 2/11/2011
- Tetra-amelia syndrome. Genetics Home Reference. February 2008; http://ghr.nlm.nih.gov/condition/tetra-amelia-syndrome. Accessed 2/11/2011.
- Genetics Home Reference (GHR) contains information on Tetra-amelia syndrome. This website is maintained by the National Library of Medicine.
- 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 Tetra-amelia syndrome. Click on the link to view a sample search on this topic.