نتایج جستجو برای: zellweger syndrome

تعداد نتایج: 622015  

Journal: :AJNR. American journal of neuroradiology 1997
A J Barkovich W W Peck

PURPOSE To determine characteristic MR imaging features of Zellweger syndrome. METHODS Clinical records, laboratory records, and MR studies of six patients with Zellweger syndrome were reviewed retrospectively. MR studies were examined for the state of myelination; the presence, extent, and morphologic appearance of cerebral cortical anomalies; the status of the cerebellar cortex, basal nucle...

Journal: :Journal of pediatric genetics 2013
David Westberry Linda Pugh

Zellweger spectrum disorders result from defects in the assembly of the peroxisome and are sometimes referred to as peroxisome biogenesis disorders. Orthopedic manifestations of this condition are variable. This case report illustrates an ambulatory child with Zellweger syndrome and progressive foot deformity. The course of treatment consisted of initial soft tissue surgery, early recurrence of...

Journal: :The Biochemical journal 1987
P Sharp A Poulos A Fellenberg D Johnson

The polyenoic fatty acids with carbon chain lengths from 26 to 38 (very-long-chain fatty acids, VLCFA) previously detected in abnormal amounts in Zellweger syndrome brain have been shown to be n-6 derivatives and therefore probably derived by chain elongation of shorter-chain n-6 fatty acids such as linoleic acid and arachidonic acid. Polyenoic VLCFA are also present in Zellweger syndrome liver...

Journal: :Journal of Medical Genetics 1996

Journal: :International Journal of Pediatrics and Adolescent Medicine 2019

Journal: :Sri Lanka Journal of Child Health 2009

Journal: :Molecular and cellular biology 2003
Megan Maxwell Jonas Bjorkman Tam Nguyen Peter Sharp John Finnie Carol Paterson Ian Tonks Barbara C Paton Graham F Kay Denis I Crane

Zellweger syndrome is the archetypical peroxisome biogenesis disorder and is characterized by defective import of proteins into the peroxisome, leading to peroxisomal metabolic dysfunction and widespread tissue pathology. In humans, mutations in the PEX13 gene, which encodes a peroxisomal membrane protein necessary for peroxisomal protein import, can lead to a Zellweger phenotype. To develop mo...

Journal: :Pediatric Neurology Briefs 1987

Journal: :Neurology India 2007
Sandra Young Yacov Rabi Abhay K Lodha

Zellweger syndrome (cerebro-hepato-renal syndrome) is associated with generalized hypotonia, high forehead with flattened facies, hepatomegaly and talipes equinovarus. This pattern of malformations was first recognized in 1964 by Bowen and Smith. Zellweger syndrome is an autosomal recessive genetic disorder that is associated with multiple biochemical markers of peroxisomal dysfunction. A full ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید