Leopard syndrome 1

Common Name(s)

Leopard syndrome 1

LEOPARD is an acronym for the manifestations of this syndrome as listed by {8:Gorlin et al. (1969)}: multiple lentigines, electrocardiographic conduction abnormalities, ocular hypertelorism, pulmonic stenosis, abnormal genitalia, retardation of growth, and sensorineural deafness. Genetic Heterogeneity of LEOPARD Syndrome LEOPARD syndrome is a genetically heterogeneous disorder. See also LEOPARD syndrome-2 ({611554}), caused by mutation in the RAF1 gene ({164760}), and LEOPARD syndrome-3 ({613707}), caused by mutation in the BRAF gene ({164757}).
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Leopard syndrome 1" for support, advocacy or research.

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Scientific Literature

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Research articles describe the outcome of a single study. They are the published results of original research.
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Clinical Trial Information This information is provided by ClinicalTrials.gov

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