Your browser does not support javascript:   Search for gard hereSearch for news-and-events here.

Diseases

Genetic and Rare Diseases Information Center (GARD)

Print friendly version

Acheiropody


Other Names for this Disease

  • Acheiropodia
  • Acheiropody, Brazilian type
  • ACHP
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

Inheritance

Newline Maker

How is acheiropody inherited?

Acheiropody is inherited in an autosomal recessive manner. This means that an individual with the condition has two changed (mutated) copies of the gene that causes the condition in each cell. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they usually do not show signs and symptoms of the condition; they are referred to as "carriers." When two people who are carriers of an autosomal recessive condition have a child, there is a 25% (1 in 4) chance that the child will have the condition, a 50% (1 in 2) chance that the child will be a carrier like each of the parents, and a 25% chance that the child will not have the condition and not be a carrier.
Last updated: 1/31/2011


Other Names for this Disease
  • Acheiropodia
  • Acheiropody, Brazilian type
  • ACHP
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.