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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.

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Q: What skin cell abnormalities are observed in patients with Zellweger syndrome?
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How is Zellweger syndrome diagnosed?

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


Is Zellweger syndrome dominant or recessive?

Zellweger syndrome is autosomal recessive.


What is the treatment for Zellweger syndrome?

There is no cure for Zellweger syndrome and treatment is based solely on lessening the symptoms and supporting the involved organs.


How may Zellweger syndrome be said to be a common condition?

The incidence of Zellweger syndrome worldwide is roughly one in 100,000 births.


How is Zellweger syndrome caused?

Zellweger syndrome is caused by mutations in any one of several different genes involved in the function of the peroxisome


Which chromosomes are affected by Zellweger syndrome?

all of them


What organelle does Zellweger syndrome affect?

peroxisomes


How is Zellweger syndrome manifest in babies?

Typically, babies with Zellweger syndrome have severe weakness, hyptonia (loss of muscle tone), and often have neonatal seizures


What causes zellweger syndrome?

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.


Can you get it from something or someone zellweger syndrome?

disease you can get from another person or animal


What is zellweger syndrome?

From wikipedia.com Zellweger syndrome, also called cerebrohepatorenal syndrome is a rare, congenital disorder (present at birth), characterized by the reduction or absence of peroxisomes (cell structures that rid the body of toxic substances) in the cells of the liver, kidneys, and brain.


How may Moebius syndrome be detected in infants?

The first sign of Moebius syndrome in newborns is an inability to suck, sometimes accompanied by excessive drooling and crossed eyes. Also seen at birth in some patients are abnormalities of the limbs