Charge syndrome is genetic. Mutations in a new member of the chromodomain gene family cause CHARGE syndrome. This syndrome is a common cause of congenital anomalies affecting several tissues in nonrandom fashion. Some research has been shown that detected mutations are in the gene CHD7 in 10 of 17 individuals with CHARGE syndrome that didn't have microdeletions, accounting for the disease in most affected individuals.
Angleman syndrome is a genetic disorder. It can be caused by 3 or 4 difference genetic malfunctions.
eyedeekaay
pedigree chart
Recessive, but dominant in some rare cases.
Noonan syndrome is caused by the mutation in a particular gene. It is a genetic disorder which means that the child which is born with this disorder, must have been in their parents.
It is genetic.
Another important genetic characteristic of Marfan syndrome is variable expression.
Angleman syndrome is a genetic disorder. It can be caused by 3 or 4 difference genetic malfunctions.
Anyone can get Marfans syndrome, it is a genetic disorder.
What specific genetic syndrome are you referring to? - for there are quite a few genetic syndromes, secondary to chromosomal duplication.
is down syndrome acquired genetic disease
yes
yes
eyedeekaay
no
There's many different genetic disorders such as: Down Syndrom Canavan Disease Muenke Syndrome Bloom Syndrome etc
Klinefelter syndrome is a genetic condition that results when a boy is born with an extra copy of the X chromosome. Klinefelter syndrome is a common genetic condition affecting males.