They are caused by the genes that we inherit from our parents. Genes govern how our body is run. Cystic fibrosis is caused by a recessive alle. This means that both parents must be carriers of the alle responsible for cystic fibrosis. The parents don't have to have the condition themselves; they can be just carriers of the one alle that makes up the condition.
Inherited diseases like hemophilia and cystic fibrosis occur due to mutations in specific genes. These mutations are passed down from parents to their offspring through their genes. Hemophilia is caused by mutations in genes responsible for blood clotting, while cystic fibrosis is caused by mutations in the CFTR gene, affecting the lungs and digestive system.
Two genetic diseases besides Down syndrome are cystic fibrosis, which affects the lungs and digestive system, and Huntington's disease, which is a neurodegenerative disorder that affects motor function and cognitive abilities.
Cystic fibrosis is one.
Cystic Fibrosis is caused by a genetic mutation in the CFTR gene. This mutation leads to the production of thick, sticky mucus in the lungs and other organs. It is not caused by a specific pathogen, but individuals with Cystic Fibrosis are more susceptible to respiratory infections.
No, cystic fibrosis affects males and females equally. It is an inherited genetic disorder caused by mutations in the CFTR gene, which can be passed down from each parent who carries a mutated gene.
Some diseases that result from inherited changes in DNA sequence include cystic fibrosis, sickle cell anemia, Huntington's disease, and Duchenne muscular dystrophy. These diseases are caused by mutations in specific genes that can be passed from parents to their offspring.
Cystic fribrosis is an inherited disease of the secretory glands, including the glands which produce sweat and mucus.
genetic disorder
gingeritus
Cystic fibrosis
Cystic Fibrosis, is a recessive disease (meaning that both parents must be carriers of the cystic fibrosis gene, for the offspring to have a chance of being born with it). A child has a 25% chance (1/4) of being born with Cystic Fibrosis.
Cystic Fibrosis
Cystic Fibrosis
Cystic Fibrosis is an example of a disease inherited as an autosomal recessive genetic disorder. Both parents of a baby who has Cystic Fibrosis have one abnormal recessive gene and one normal dominant gene and are therefore, Cystic Fibrosis carriers. Carriers are said to be heterozygous because they contain one normal copy of the gene and one abnormal copy. A baby who inherits cystic fibrosis has inherited the abnormal gene from both parents and is therefore said to be homozygous recessive.
-Cystic Fibrosis -Hemophilia -Tay-Sachs disease
Cystic fibrosis can't be "caught". It is an inherited disease passed down in the genes to family members.
infection cystic fibrosis inherited treatment ministration cystic fibrosis is a genetic disorder which affects the lungs and pancreas's
Two genetic diseases besides Down syndrome are cystic fibrosis, which affects the lungs and digestive system, and Huntington's disease, which is a neurodegenerative disorder that affects motor function and cognitive abilities.