Tetra-amelia syndrome

Tetra-amelia syndrome (tetra- + amelia), also called autosomal recessive tetraamelia,^[1] is an extremely rare autosomal recessive^[2] congenital disorder characterized by the absence of all four limbs. Other areas of the body are also affected by malformations, such as the face, skull, reproductive organs, anus and pelvis.^[1] The disorder is caused by mutations in the WNT3 gene.^[2]

Characteristics

Tetra-amelia syndrome is characterized by the complete absence of all four limbs. The syndrome causes severe malformations of various parts of the body, including the face and head, heart, nervous system, skeleton, and genitalia. In many cases, the lungs are underdeveloped, 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.

Cause and genetics

Tetra-amelia syndrome has an autosomal recessive pattern of inheritance.

The WNT3 Gene

Researchers have found a mutation in the WNT3 gene in people with tetra-amelia syndrome from one large family. This gene is part of a family of WNT genes that play critical roles in development before birth. The WNT3 gene is located at human chromosome 17q21.^[3]

The protein produced from the WNT3 gene is involved in the formation of the limbs and other body systems during embryonic development. Mutations in the WNT3 gene prevent cells from producing functional WNT3 protein, which disrupts normal limb formation and leads to the other serious birth defects associated with tetra-amelia syndrome.

Genetics within families

In some affected families, the cause of tetra-amelia syndrome has not been determined. Some researchers believe that unidentified mutations in WNT3 or other genes involved in limb development may be responsible for the disorder.

In most of the families reported so far, tetra-amelia syndrome appears to have an autosomal recessive pattern of inheritance.^[1][2] This means the defective gene responsible for the disorder is located on an autosome (chromosome 17 is an autosome), and two copies of the defective gene (one inherited from each parent) are required in order to be born with the disorder. The parents of an individual with an autosomal recessive disorder both carry one copy of the defective gene, but usually do not experience any signs or symptoms of the disorder.

Epidemiology

Tetra-amelia syndrome has been reported in only a few families worldwide. According to a 2011 study by Bermejo-Sanchez, tetra-amelia occurs in roughly 1 out of every 71,000 pregnancies.^[4]

People with tetra-amelia syndrome

• Nick Vujicic, founder of Life Without Limbs ^[5]
• Joanne O'Riordan of Millstreet, Cork, Ireland. At the age of 16 she addressed the United Nations in New York. She appeared before the International Telecommunication Union’s conference ‘Girls in Technology’, receiving a standing ovation after delivering the keynote speech.
• Hirotada Ototake
• Prince Randian
• Violetta (entertainer)

Nick Vujicic, a motivational speaker who was born with Tetra-amelia syndrome, speaking during the session "Inspired for a Lifetime" at the Annual Meeting 2011 of the World Economic Forum in Davos, Switzerland, on 30 January 2011 ^{[6] [7]}

References

External links

• "Tetra-amelia syndrome - Genetics Home Reference". U.S. National Library of Medicine. Retrieved 2009-01-09. 
• "Tetra-Amelia Syndrome -- GeneReviews -- NCBI Bookshelf". University of Washington, Seattle. Retrieved 2009-01-09. 
• "Tetra-Amelia-Syndrome (Birth defects & disorders)". I-Am-Pregnant. Retrieved 2009-01-09. 
• "Tetraamelia multiple malformations - WrongDiagnosis.com". WrongDiagnosis. Retrieved 2009-01-09. 
• Life Without Limbs