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Triploid syndrome, also called triploidy, is a chromosomal disorder in which a fetus has three copies of every chromosome instead of the normal two. If this occurs in only some cells, it is called mosaic triploidy and is less severe. Most embryos with triploidy miscarry early in development.
Polyploidy is a condition in which the cells of an organism have more than two paired sets of chromosomes. Most species whose cells have nuclei ( eukaryotes ) are diploid , meaning they have two complete sets of chromosomes, one from each of two parents; each set contains the same number of chromosomes, and the chromosomes are joined in pairs ...
Diploid-triploid mosaicism is a human chromosome disorder.Individuals with diploid-triploid syndrome have some cells with three copies of each chromosome for a total of 69 chromosomes (called triploid cells) and some cells with the usual 2 copies of each chromosome for a total of 46 chromosomes (called diploid cells).
Triploid organisms, for instance, are usually sterile. Because of this, triploidy is commonly exploited in agriculture to produce seedless fruit such as bananas and watermelons. If the fertilization of human gametes results in three sets of chromosomes, the condition is called triploid syndrome. [citation needed]
The basic number of chromosomes in the somatic cells of an individual or a species is called the somatic number and is designated 2n. In the germ-line (the sex cells) the chromosome number is n (humans: n = 23). [4] [5] p28 Thus, in humans 2n = 46. So, in normal diploid organisms, autosomal chromosomes are present in two copies.
This is an accepted version of this page This is the latest accepted revision, reviewed on 3 December 2024. Union of gametes of opposite sexes during the process of sexual reproduction to form a zygote This article is about fertilisation in animals and plants. For fertilisation in humans specifically, see Human fertilization. For soil improvement, see Fertilizer. "Conceive" redirects here. For ...
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It is named after American endocrinologist Harry Klinefelter, who identified the condition in the 1940s, along with his colleagues at Massachusetts General Hospital. [ 4 ] [ 5 ] [ 11 ] [ 12 ] The syndrome is defined by the presence of at least one extra X chromosome in addition to a Y chromosome , yielding a total of 47 or more chromosomes ...