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Trisomy 18 is a form of chromosomal aberration. It is neither recessive nor dominant. Neither does it show co-dominance or incomplete dominance factor. It arises due to the presence of an extra chromosome 18 in the somatic cells.

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14y ago
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15y ago

None of these!

"Trisomy" means that there are three copies of a particular chromosome, so trisomy 13 is characterized by three copies of chromosome 13.

There are two causes of trisomy:

During meiosis I, homologous chromosomes, such as the two copies of number 13, should separate at anaphase. Sometimes both copies go to the same pole, eventually resulting in a gamete with one copy too many of the chromosome. At fertilization, this nucleus is paired with that of a regular gamete, forming a zygote with trisomy.

Parts of chromosomes may break and combine with other chromosomes. This is called translocation. In particular, one type, Robertsonian translocation, affects chromosomes whose centromeres are near one end of the chromosome, namely chromosomes 13, 14, 15, 21, and 22.

Trisomy 13 can result from one gamete inheriting both a regular copy of chromosome 13 and another chromosome (usually 14) carrying an additional long arm (q) of chromosome 13. When this gamete combines with a normal gamete, the zygote inherits two copies of chromosome 13, plus a third copy of most of the genes in chromosome 13. Photos of children with Robertsonian translocation off the LWT13 website. Use the SEARCH option for Translocation. http://www.livingwithtrisomy13.org

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15y ago

dominant

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Q: Is trisomy 13 inherited by a dominant or recessive trait or is it sex linked?
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