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Lellweger Syndrome Lellweger Syndrome

Lellweger Syndrome - PDF document

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Uploaded On 2022-08-22

Lellweger Syndrome - PPT Presentation

Zellweger Syndrome belongs to a group of disorders known as leukodystrophies Jt is a rare disorder that is apparent from bir th Jt results from a failure to assemble subcellular structures known as ID: 939726

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Lellweger Syndrome Zellweger Syndrome belongs to a group of disorders known as leukodystrophies. Jt is a rare disorder that is apparent from bir th. Jt results from a failure to assemble subcellular structures known as peroxisomes. These are important cellular structures responsible for removing toxic substances from within cells. They are found in the cells of the liver, kidneys and the brain . Zellweger Syndrome is the most severe form of a class of condi�ons referred to as peroxisomal biogenesis disorders. The disorder is characterised in infancy by low muscle tone, feeding problems, sight and hearing loss, and seizures. Synonyms Alterna�ve names for this condi�on are: • Bowen Syndrome • Cerebrohepatorenal Syndrome Further informa�on about this condi�on is available from Climb. Disclaimer slease read our disclaimer and informa�on on data protec�on . ClimbHu ClimbHu TeamClimb Telephone: 0845 241 2173 Freephone: 0800 652 3181 Email: contact@climb.org.uk Website: www.climb.org.uk Children Living with Jnherited Metabolic Diseases is a charity registered in England and Wales (1089588) in Scotland (SC044634) and a Company Limited by Guarantee 4267454 Join our Family Contacts Network Updated 07/04/17