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Sjogren-Larsson Syndrome (SLS) clinical trials

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NCT ID: NCT01971957 Completed - Clinical trials for Sjogren-Larsson Syndrome (SLS)

Sjogren-Larsson Syndrome: Natural History, Clinical Variation and Evaluation of Biochemical Markers

SLS
Start date: April 1, 2013
Phase:
Study type: Observational [Patient Registry]

Sjogren-Larsson syndrome (SLS) is a rare genetic disease in which patients typically exhibit ichthyosis (dry, scaly skin), intellectual disability, spasticity, seizures and a distinctive maculopathy. The purpose of this study is to define the clinical spectrum and natural history of Sjogren-Larsson syndrome, and identify biomarkers that correlate with disease phenotype while establishing a registry for future investigations of biochemical pathogenesis and therapy.