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About Lowe Syndrome

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Lowe Syndrome (OCL Syndrome, Oculo-Cerebro-Renal Dystrophy) is a rare genetic condition in boys which affects eyes, kidneys and the brain.

Lowe Syndrome is associated with mild to severe learning disabilities and speech delay.

Children are born with cataracts and undergo surgery early in life to remove them. Lowe Syndrome is also associated with glaucoma and around 50% of individuals will require on-going treatment. Visual impairment is generally within the range that can be corrected by glasses and/or contact lenses.

Around half of boys with Lowe Syndrome are affected by epilepsy.

Physical difficulties include problems related to weak muscles, brittle bones and poor fine & gross-motor coordination.

Behavioural and social problems akin to autistic spectrum disorder are frequent, if not general.



  • Lowe Syndrome Association
    A US based international support organisation maintaining an excellent reference site on Lowe Syndrome.
     
  • Lowe Syndrome Trust
    An energetic UK Charity providing support and information to families, individuals and professionals affected by Lowe Syndrome
     
  • Educational Issues from LSA
    An article from the Lowe Syndrome Association summarising developmental and education issues for boys with Lowe Syndrome.
     
  • OMIM Reference
    Clinical references on Lowe Syndrome from the OMIM database.