Genetic disorders can be classified according to the way in which they develop. If the disorder is transmitted by genes inherited from only one parent, it is said to be an autosomal dominant disorder. The term autosome applies to any of the 22 chromosomes that are identical in human males an...
Other examples of genetic congenital disorders include: Sickle cell disease, genetic mutation causes a change in the red blood cells shape when they are deprived of oxygen. Cystic Fibrosis, a condition associated with very poor lung function Marfan Syndrome, a connective tissue disorder leading to ...
Single gene trait examples include eye color, presence of freckles or dimples, type of ear lobe, and widow's peak hairline. How are single gene disorders inherited from parents? If a genetic disorder is linked to the dominant allele, a child can inherit the disease from parents even if just...
The analysis of this diseasome revealed that IDPs are abundant in proteins linked to human genetic diseases, and that different genetic disease classes varied dramatically in the IDP content (Midic U., Oldfield C. J., Dunker A. K., Obradovic Z., Uversky V. N. (2009) Protein disorder in...
As a result of nondisjunction in one of the daughter cells of Meiosis II, when the gamete with the extra chromosome combines with a normal gamete, what type of genetic disorder results? Is Down syndrome an autosomal or carried on the sex chromosomes (X, Y). Exp...
In terms of phenotype, the hybrids are long pea plants, thus indicating that the tall trait is the dominant trait and the short trait is a recessive trait. 2. Huntington’s Disease Huntington’s disease is a condition resulting from a genetic disorder. The disease is caused by the Huntingtin...
Autosomal disorders result from different types of genetic alterations: Point mutations Insertions Deletions Chromosomal rearrangements Repeat expansions The specific genetic alteration depends on the disorder and can affect coding regions, regulatory elements, or non-coding regions of the gene. ...
For instance, in medicine, the availability of training data can greatly diminish when it comes to rare diseases or advanced clinical research. This is the case of X-linked Agammaglobulinemia (XLA), which is a rare genetic disorder characterized by the lack of B cells in the immune system,...
Checking for the possibility of genetic disorder is the reason for repeated miscarriages in any women Checking for a genetic disorder in a stillborn child for identifying the cause of death Rule out the possibility of any congenital disease in an offspring ...
This occurs via a method known as DNA methylation, which does not alter the genetic sequence itself. What is a genomic imprinting disorder? A genomic imprinting disorder involves the imprinting of a region that is supposed to be expressed. For example, Prader-Willi syndrome involves the ...