NINDS Zellweger Syndrome Information Page: NINDS
Article title: NINDS Zellweger Syndrome Information Page: NINDS
Main condition: Zellweger Syndrome
Conditions: Zellweger Syndrome
Table of Contents (click to jump to sections)
What is Zellweger Syndrome?
Is there any treatment?
What is the prognosis?
What research is being done?
Organizations
What is Zellweger Syndrome?
Zellweger syndrome is a rare, congenital (present at birth) disorder 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. Zellweger syndrome is one of a group of genetic disorders called peroxisomal diseases that affect brain development and the growth of the myelin sheath, the fatty covering—which acts as an insulator—on nerve fibers in the brain. The most common features of Zellweger syndrome include an enlarged liver, high levels of iron and copper in the blood, and vision disturbances. Some affected infants may show prenatal growth failure. Symptoms at birth may include lack of muscle tone and an inability to move. Other symptoms may include unusual facial characteristics, mental retardation, seizures, and an inability to suck and/or swallow. Jaundice and gastrointestinal bleeding may also occur.
Is there any
treatment?
There is no cure for Zellweger syndrome, nor is there a
standard course of treatment. Infections should be guarded against to
prevent such complications as pneumonia and respiratory distress. Other
treatment is symptomatic and supportive.
What is the prognosis?
The
prognosis for individuals with Zellweger syndrome is poor. Death usually
occurs within 6 months after onset, and may be caused by respiratory
distress, gastrointestinal bleeding, or liver failure.
What research is being
done?
The NINDS supports research on genetic disorders including
leukodystrophies such as Zellweger syndrome. The goals of this research
are to increase scientific understanding of these disorders, and to find
ways to prevent, treat, and cure them.
National Institute of Child Health and Human Development
(NICHD)
National Institutes of Health
Bldg. 31, Rm. 2A32
Bethesda, MD 20892-2425
NICHDClearinghouse@mail.nih.gov
http://www.nichd.nih.gov/
Tel:
301-496-5133 800-370-2943
National Organization for Rare Disorders (NORD)
P.O. Box 8923
(100 Route 37)
New Fairfield, CT 06812-8923
orphan@rarediseases.org
http://www.rarediseases.org/
Tel:
203-746-6518 800-999-NORD (6673)
Fax: 203-746-6481
United Leukodystrophy Foundation
2304 Highland Drive
Sycamore, IL 60178
ulf@tbcnet.com
http://www.ulf.org/
Tel: 815-895-3211
800-728-5483
Fax: 815-895-2432
This fact
sheet is in the public domain. You may copy it.
Provided by:
The National Institute of Neurological Disorders and Stroke
National Institutes of Health
Bethesda, MD 20892
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