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What is the most common chromosomal abnormality in humans?
The most common chromosomal abnormality in humans is Down syndrome, which is caused by an extra copy of chromosome 21. It occurs in about 1 in 700 births.
Is 5p syndrome caused by a chromosomal abnormality?
Yes, 5p syndrome, also known as Cri du Chat syndrome, is caused by a chromosomal abnormality involving a deletion of a portion of the short arm of chromosome 5. This genetic alteration leads to a range of developmental and physical challenges, including distinctive cat-like cry in infants, intellectual disability, and various physical abnormalities. The severity of symptoms can vary widely depending on the size and location of the deletion.
What is the karyotype of klienfeter syndrome?
Individuals with Klinefelter syndrome typically have an extra X chromosome, resulting in a karyotype of 47,XXY. This chromosomal abnormality can cause developmental and reproductive issues in affected individuals.
Who discovered 47 XYY?
The discovery of the 47 XYY syndrome was first reported by Patricia A. Jacobs and J.A. Strong in 1961. They described a male with an extra Y chromosome, leading to the identification of this chromosomal abnormality.
Is turner syndrome inheritable or random?
Turner syndrome is usually random and not inherited. It occurs when a female is born with a missing or incomplete X chromosome. In rare cases, Turner syndrome can be inherited if one parent carries a chromosomal abnormality.
Is anyone susceptible to this Down syndrome?
no, it is a chromosomal abnormality, not a contagious disease.
What is the medical term of trisomy 16?
It is called Patau syndrome and is a chromosomal abnormality
What is the most common chromosomal abnormality in humans?
The most common chromosomal abnormality in humans is Down syndrome, which is caused by an extra copy of chromosome 21. It occurs in about 1 in 700 births.
What chromosomal abnormality causes Klinefelter syndrome?
46,XXY or XXY for males; see the link below.
What chromosomal abnormality causes Turner syndrome?
If one of sex chromosomes is missing. Normal-XX Turner- XO
What is the male version of Rett syndrome called?
Rett syndrome in boys is known as Rett syndrome. Male fetuses with Rett syndrome do not typically survive until birth unless they have an extra X chromosome (XXY).
What is meant by chromosomal abnormality?
Chromosomal abnormality is a broader term, describing duplications, loss, gain etc, of a particular chromosome. More related to the structures in an ideogram.Genetic disorder is a much broader term that describes any chromosomal or genetic changes. A disease condition.
Does Clint Black have a relative with rett syndrome?
Yes, his niece Courtney has rett syndrome.
If the disease is a chromosomal abnormality describe the abnormality?
what is the answer to this question
When was Rett syndrome discovered?
Andreas rett
What gene is affected in Down Syndrome?
It is the result of a chromosomal abnormality, in which there is an extra chromsome on the chromosome 21 pair. This is call trisomy 21.
Is marfan syndrome a chromosomal abnormality?
No, Marfan syndrome is not a chromosomal abnormality. It is a genetic disorder caused by a mutation in the fibrillin-1 (FBN1) gene, which affects the body's connective tissue. This gene is located on chromosome 15.
