Tetra-amelia syndrome
is inherited in an ‘autosomal recessive manner’. Autosomal recessive
inheritance means both copies of the gene in each cell have mutations. The
parents of an individual with tetra-amelia syndrome each carry one copy of the
mutated gene, but do not show signs and symptoms of the condition.
At conception, each
sib of an affected individual has a 25%
chance of being affected, a 50% chance of being an asymptomatic carrier, and a 25% chance of being unaffected and
not a carrier. Heterozygotes (carriers) are asymptomatic.
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