all of them
Zellweger syndrome is autosomal recessive.
#21
Zellweger syndrome is a rare genetic disorder with an estimated prevalence of 1 in 50,000 to 1 in 100,000 births. This translates to less than 0.001% of the population being affected by Zellweger syndrome.
chromosome 21
The incidence of Zellweger syndrome worldwide is roughly one in 100,000 births.
There is no cure for Zellweger syndrome and treatment is based solely on lessening the symptoms and supporting the involved organs.
The chromosomes which are affected in Turner's Syndrome is the sex chromosomes. A normal female individual has 2 X sex chromosomes. In Turner's Syndrome, a woman only has one X chromosome and is missing the other. Thus, a woman with Turner's Syndrome has the sex chromosomes X0.
Typically, babies with Zellweger syndrome have severe weakness, hyptonia (loss of muscle tone), and often have neonatal seizures
Zellweger syndrome is caused by mutations in any one of at least 12 genes ; mutations in the PEX1 gene are the most common cause. It is inherited in an autosomal recessive manner. There is no cure for Zellweger syndrome; treatment is generally symptomatic and supportive.
Either chromosome 13 or 7. Mostly 13
Yes, Non-disjunction occurs when sex chromosomes fail to separate. This occurrence leads to variable numbers of chromosomes and the manifestation of developmental diseases such as Down syndrome, Turner syndrome, etc.
Forty-seven. In Down syndrome, there is an extra 21st chromosome. It is also known as Trisomy 21.