Zellweger Syndrome

Zellweger Syndrome
This syndrome is named after Hans Ulrich Zellweger, a Swiss-American pediatrician who first described it.

Zellweger Syndrome
Medical Dictionary
Definition of medical terminology for Zellweger Syndrome.

NINDS Zellweger Syndrome Information Page
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Zellweger Syndrome
Zellweger Syndrome is a rare, autosomal recessive congenital syndrome of multiple abnormalities.

Zellweger syndrome (cerebrohepatorenal syndrome)
Brain and liver defects
Developmental delay ...

zellweger syndrome
Zieve's syndrome
Zivert syndrome
Zollinger-Ellison syndrome ...

Zellweger Syndrome ... low birth weight, prenatal growth failure
Conditions listing medical complications: Pregnancy symptoms: ...

Individuals with Zellweger syndrome develop signs and symptoms of the condition during the newborn period. These infants experience weak muscle tone (hypotonia), feeding problems, hearing loss, vision loss, and seizures.

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Cerebrohepatorenal syndrome: A genetic disorder, which is also called the Zellweger syndrome, characterized by the reduction or absence of peroxisomes (cell structures that rid the body of toxic substances) in the cells of the liver, ...

the deletion syndromes involving chromosomes 4p, 4q, 5p (cat cry syndrome), and 18q; the fetal alcohol syndrome; Seckel syndrome; Smith-Lemli-Opitz syndrome; the syndromes due to trisomy 13 (Patau syndrome) and trisomy 8; and Zellweger syndrome.

See also: Symptom, Autosomal recessive, Kidney, Cancer, Stroke