Persons with Zellweger syndrome rarely live more than one year after diagnosis, with death due mostly to severe feeding difficulties, liver complications, respiratory distress, and cardiac defects.
Zellweger syndrome is autosomal recessive.
The prognosis of individuals with Lambert-Eaton myasthenic syndrome varies widely. In fact, the most important element of prognosis involves the prognosis associated with any existing cancer.
The prognosis of individuals with Lambert-Eaton myasthenic syndrome varies widely. In fact, the most important element of prognosis involves the prognosis associated with any existing cancer.
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
peroxisomes
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.
Persons with carpal tunnel syndrome can usually expect to gain significant relief from prescribed surgery, treatments, exercises, and positioning devices.
The prognosis for males diagnosed with Wiskott-Adrich syndrome is poor.