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Can 46xx be male phenotype?
No, 46,XX karyotype is typically associated with a female phenotype due to the presence of two X chromosomes. This combination usually leads to female sexual development.
Does turner's syndrome occur in all cells?
No, only the gametes would be indicative of sterility. It is possible that the individual (though incredibly rare) to have "chimera" syndrome, where two non-identical twins merge to form one fetus. Turner's Syndrome is the absence of the male sex chromosome BTW. That chromosome carries little genetic information, and is possible during mitosis to "loose" it, but still create a mostly viable cell.
Turner's syndrome describe the genetic makeup of someone with this disorder?
Turner syndrome is characterized by the absence of all or part of one of the X chromosomes in females, leading to short stature and various medical issues. Most individuals with Turner syndrome have a karyotype of 45,X, meaning they have only one X chromosome.
What are characteristics of Turners syndrome?
Depending on the type of Turner syndrome a person has, their karyotype is either: 45X - classic Turner syndrome - second X chromosome missing from all cells 45X/46XX - Mosaic Turner syndrome - second X chromosome missing from some cells. There is another type of Turner syndrome, but it has a more complicated karyotype and I am not sure what the karyotype is off the top of my head.
Are there different types of turner syndrome?
There are 3 types of Turner syndrome Classic Turner syndrome - 45X - second X chromosome missing from all cells. Mosaic Turner syndrome - 45X/46XX - second X chromosome missing from some cells. The third type of Turner syndrome is when the second X chromosome is damaged or only partly missing.
Can 46xx be male phenotype?
No, 46,XX karyotype is typically associated with a female phenotype due to the presence of two X chromosomes. This combination usually leads to female sexual development.
What does karytype mean?
Karyotype refers to genetic testing. A karyotype is a pictorial analysis of the number, form, and size of an individual's chromosomes. Cells from any nucleated replicating body tissue (except red blood cells, nerves or muscles) can be used for testing. The most commonly used tissues are white blood cells and fetal cells in amniotic fluid. The female karyotype is 46XX chromosomes and the male karyotype is 46XY chromosomes. Karyotypes can be used to determine the sex of a child and the presence of any gross chromosomal abnormalities
Does turner's syndrome occur in all cells?
No, only the gametes would be indicative of sterility. It is possible that the individual (though incredibly rare) to have "chimera" syndrome, where two non-identical twins merge to form one fetus. Turner's Syndrome is the absence of the male sex chromosome BTW. That chromosome carries little genetic information, and is possible during mitosis to "loose" it, but still create a mostly viable cell.
Turner's syndrome describe the genetic makeup of someone with this disorder?
Turner syndrome is characterized by the absence of all or part of one of the X chromosomes in females, leading to short stature and various medical issues. Most individuals with Turner syndrome have a karyotype of 45,X, meaning they have only one X chromosome.
What is the normal genotype for a human female 44XX or 46XX?
The normal genotype for a human female is 46XX, meaning she has 46 chromosomes, including two X chromosomes. A genotype of 44XX would be considered abnormal in humans.
What are characteristics of Turners syndrome?
Depending on the type of Turner syndrome a person has, their karyotype is either: 45X - classic Turner syndrome - second X chromosome missing from all cells 45X/46XX - Mosaic Turner syndrome - second X chromosome missing from some cells. There is another type of Turner syndrome, but it has a more complicated karyotype and I am not sure what the karyotype is off the top of my head.
Are there different types of turner syndrome?
There are 3 types of Turner syndrome Classic Turner syndrome - 45X - second X chromosome missing from all cells. Mosaic Turner syndrome - 45X/46XX - second X chromosome missing from some cells. The third type of Turner syndrome is when the second X chromosome is damaged or only partly missing.
What does the karyotype of a person with turners syndrome look like?
There are a few types of Turner syndrome. The most common two are: 1) Classic - The karyotype is 45X. The second X chromosome in missing from all cells. 2) Mosaic - The karotype is 45X/46XX. The second X chromosome is missing from some cells. 3) There are other types of Turner syndrome in which the second X is only partly missing or it is partly damaged.
How many chromosomes does a praying mantis have?
All organisms contain 46 chromosomes. A praying mantis will also have 46 chromosomes. The males have 46XX and the females 46XY.
Turner's syndrome individuals have which genotype?
Individuals with Turner syndrome typically have a genotype of 45,X, meaning they only have one X chromosome instead of the usual two. This genetic condition affects women and is associated with various physical and developmental differences.
What is the genotype for a girl with turners syndrome?
Genotype-1 'X' chromosomePhenotype-Short statureLymphedema(swelling) of the hands and feetBroad chest (shield chest) and widely spaced nipplesLow hairlineLow-set earsReproductive sterilityRudimentary ovaries gonadal streak (underdeveloped gonadal structures that later become fibrosed)Amenorrhoea, or the absence of a menstrual periodIncreased weight, obesityShield shaped thorax of heartShortened metacarpal IVSmall fingernailsCharacteristic facial featuresWebbed neck from cystic hygroma in infancyCoarctation of the aortaBicuspid aortic valvePoor breast developmentHorseshoe kidneyVisual impairments sclera, cornea, glaucoma, etc.Ear infections and hearing lossHigh waist-to-hip ratio (the hips are not much bigger than the waist)Attention Deficit/Hyperactivity Disorder or ADHD (problems with concentration, memory, attention with hyperactivity seen mostly in childhood and adolescence)Nonverbal Learning Disability (problems with math, social skills and spatial relations)
How many chromosomes do hermaphrodites have?
Hermaphrodites can have a variety of chromosome combinations, depending on the species. In humans, individuals with both male and female reproductive organs (a type of intersex condition) typically have the usual chromosome pair of 46, but may have variations such as XXY or XYY. In other species, such as earthworms or snails, hermaphrodites may have different numbers of chromosomes.
