Tay-Sach's Disease/
yes it is. It affects chromosome 11.
Yes, Duchenne muscular dystrophy is a genetic disorder caused by mutations in the dystrophin gene. It is inherited in an X-linked recessive manner, meaning it primarily affects males and can be passed down from carrier females.
Rett syndrome is a rare genetic disorder that is typically caused by a mutation in the MECP2 gene located on the X chromosome. It is not classified as dominant or recessive in the traditional sense because it primarily affects individuals with two X chromosomes. It is considered an X-linked dominant disorder with variable expressivity and reduced penetrance.
Yes, hemophilia is an inherited disorder that affects blood clotting. It is primarily caused by a deficiency in specific clotting factors, with hemophilia A resulting from a lack of factor VIII and hemophilia B from a lack of factor IX. The condition is usually passed down through families in an X-linked recessive pattern, primarily affecting males. As a result, individuals with hemophilia experience prolonged bleeding and difficulty forming blood clots.
Marfan's Syndrome is inherited in an autosomal dominant pattern. This disease is a disorder that affects the connective tissue in many parts of the body.
That is hemophilia. It primarily affects males because females with hemophilia do not survive past menarche. The will bleed to death with their first menstruation.
Yes, hemophilia A is a sex-linked recessive genetic disorder caused by a mutation in the F8 gene on the X chromosome. It primarily affects males, who inherit the defective gene from their mothers. Females can be carriers of the gene and may pass it on to their children.
Yes, the disorder you are referring to is hemophilia A, which is caused by a deficiency or missing factor VIII in the blood. This results in impaired blood clotting and leads to prolonged bleeding after injury or surgery. It is inherited in an X-linked recessive pattern, meaning it predominantly affects males.
Duchenne muscular dystrophy is the disorder characterized by a lack of protein dystrophin. This genetic disorder affects muscle function and leads to progressive muscle weakness and degeneration. It primarily affects boys and can result in mobility issues and other complications.
Duchenne Muscular Dystrophy is more commonly seen in males of all ethnicities. It is an X-linked recessive disorder that primarily affects males because the gene mutation responsible for the condition is located on the X chromosome.
Cystic fibrosis is a recessive genetic disorder that affects chloride ion uptake in cells, leading to an osmotic imbalance and excess mucus production in various organs, particularly affecting the lungs and digestive system. This can lead to breathing difficulties, frequent lung infections, and problems with digestion and nutrient absorption.
what disorder primary affects the bone matrix and is due to the loo of calcium salt