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Clinical and Molecular Aspects of Sjogren-Larsson Syndrome Reported in an Iranian Consanguineous Family with Triplet Affected Individuals
Sjogren-Larsson Skin disease Mutation Iran
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2015/9/25
Background: Sjogren Larsson Syndrome (SLS; OMIM: 270200) is an autosomal recessive neuro-cutaneous disorder characterized by mental retardation, congenital ichthyosis and spastic paraplegia. SLS is ca...
The Exclusion of Sjögren-Larsson Syndrome in High Risk Pregnancy Using Enzimatic Methods
Sjö gren-Larsson Syndrome High Risk Pregnancy Enzimatic Methods
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2009/7/3
Sjogren-Larsson Syndrome (SLS) is an inherited neurocutaneous disorder characterized by mental
retardation, spasticity and ichthyosis. Since it was first described in 1957, over 200 patients have bee...