peroxisomes
I know a girl with Z's and she just turned 18.
Its in the Genes, not that shorts ;-)
For example,if the nucleus is absent,then the cell and its functions cannot be controlled.If the endoplsmic reticulum is absent, then the food cannot be transported in the cell.This shows that the absence of an one organeele will adversely affect the working of the cell.
cryptorchidism which is undescended testicles in males is one example
Yes it is an organelle.
Zellweger syndrome is autosomal recessive.
Ribosomes
Mitochondria
There is no cure for Zellweger syndrome and treatment is based solely on lessening the symptoms and supporting the involved organs.
The incidence of Zellweger syndrome worldwide is roughly one in 100,000 births.
Zellweger syndrome is caused by mutations in any one of several different genes involved in the function of the peroxisome
all of them
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.
in Zellweger syndrome, these cells appear to have ghost-like peroxisomes, which are caused by an absence of specific proteins inside the organelles that are recruited into the membranes.
disease you can get from another person or animal
Zellweger syndrome is diagnosed by measuring metabolic compounds in blood samples from patients. Various fatty acids, plasmalogens, pipecolic acid, and bile acid intermediates are usually studied