Cistic Fibrosis is when Mucus clots up in the lungs and intestines making it harder to breath. =)
No, achondroplasia is not caused by nondisjunction. Achondroplasia is a genetic disorder caused by a spontaneous mutation in a gene involved in bone growth. Nondisjunction is a genetic event that occurs during cell division and can lead to abnormal chromosome numbers in offspring.
Cells grow and divide at an abnormally high rate in cancer. This uncontrolled growth leads to the formation of tumors.
No, progeria is not caused by non disjunction. Progeria is a rare genetic disorder where a mutation occurs in the LMNA gene, leading to premature aging in children. Non disjunction is a different type of genetic error where chromosomes fail to separate properly during cell division.
Turner Syndrome is a genetic disorder that affects females only. It is caused by the absence of all or part of one of the X chromosomes. This condition is not passed down through family genetics, but occurs randomly.
The question is not proper. Please define more. I assume you meant whether the genetic information is transferred between homologous chromosomes. Yeah it does. When the two homologous chromosomes pair up to form bivalents, crossing over occurs between them.
genetic disorder
Sickle Cell Anemia
The main effect is on the tides, when the sun and moon are at right angles it produces neap tides. When in line it produces spring tides. Spring tides are abnormally high, neap tide are abnormally low
Sickle cell anemia is a genetic disorder that primarily occurs in African Americans. It is caused by a mutation in the gene that makes hemoglobin, resulting in abnormal red blood cells that can cause blockages in blood vessels and organ damage.
i believe all types of haemophilia are genetic although i am not sure. but i do know that CLASSIC HAEMOPHILIA is a genetic disorder Haemophilia A and B are both genetic. Haemophilia A (which is the most common) occurs when your blood lacks a clotting agent called factor 8. Haemophilia B occurs when you lack factor 9 in your blood. There is also acquired Haemophilia, this occurs when the immune system starts attacking clotting agents within the blood, this usually occurs in elderly people. Both forms of genetic haemophilia mostly occur in males, it rarely occurs in females. Unfortunately there is no cure but it is quite easily controlled with injections of the missing clotting agent.
Marfan's syndrome is the most common genetic disorder of connective tissue. It occurs in about every 10,000 to 20,000 individuals.
An example of a genetic disorder that is both genetic and congenital is Down syndrome, also known as trisomy 21. It is caused by the presence of an extra copy of chromosome 21, which occurs at conception. This condition is present at birth and is associated with various physical and developmental challenges. Other examples include cystic fibrosis and sickle cell disease, which also arise from genetic mutations and manifest at birth.
No, because this genetic disorder occurs because the parents are heterozygous, they don't show any symptoms. However, if each pqarent passes the recessive allele to the child, the child inherits both recessive alleles and will have a recssive genetic disorder, so it doesnt matter if you have a gene transfer because, the new gene is not yours, so you children may have it. xoxo
No, achondroplasia is not caused by nondisjunction. Achondroplasia is a genetic disorder caused by a spontaneous mutation in a gene involved in bone growth. Nondisjunction is a genetic event that occurs during cell division and can lead to abnormal chromosome numbers in offspring.
an error in meiotic cell division
Cleft lip and palate is not a sex-linked disorder. It is a common birth defect that occurs due to both genetic and environmental factors, with a multifactorial inheritance pattern involving multiple genes as well as environmental influences.
A fatal genetic disorder in which metabolic wastes build up in the body is known as a lysosomal storage disorder. This group of disorders occurs when there is a deficiency of enzymes needed to break down various substances in cells, leading to the accumulation of these substances in the body, causing damage to tissues and organs. Examples include Tay-Sachs disease and Gaucher disease.