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It is a disease/disorder that occurs more in families than by chance alone. (i.e. it is hereditary in cause or susceptibility)

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Q: What is a familial disorder?
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What are the characteristics of familial polyposis?

Familial polyposis or familial adenomatous polyposis (FAP) is a premalignant disease. This means that a person with FAP, if left untreated, will invariably develop cancer. Individuals with this disorder grow hundreds of polyps.


What is the familial or the sporadic migraine?

Familial means hereditary, running in families, hence predictable at times. Sporadic means randomly caused, with no heredity that an be traced, usually by a mutation in the same gene that causes the familial form of the disorder.


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Is Familial polyposis cancerous?

Hello, I see you are asking "Is Familial polyposis cancerous" Familial adenomatous polyposis (FAP) is an inherited disorder characterized by cancer of the large intestine (colon ) and rectum. People with the classic type of familial adenomatous polyposis may begin to develop multiple noncancerous (benign) growths (polyps ) in the colon as early as their teenage years. To get more info visit the url: orthopedicshealth. com/symptoms/directory/a


What is an autosomal dominant disorder that results in a defective or deficient LDL receptor known as?

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What has the author Jennifer Crosbie written?

Jennifer Crosbie has written: 'Inhibition as a marker for a familial subgroup of Attention Deficit Hyperactivity Disorder' -- subject(s): Inhibition in children, Attention-deficit hyperactivity disorder 'Genetic risk and phenotypic variation in attention deficit hyperactivity disorder' -- subject(s): Attention-deficit hyperactivity disorder, Genetic aspects, Genetic aspects of Attention-deficit hyperactivity disorder, Phenotype


When was Familial - album - created?

Familial - album - was created in 2001.


What does the medical term familial mean?

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We invited my grandparents over for a familial Christmas dinner.


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A normal couple has 5 children 2 of whom suffered from somewhat uncommon genetic disorder that has however appeared sporadically in this familial line what kind of gene is responsible for this case?

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