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Joubert syndrome 35

Summary

Joubert syndrome-35 (JBTS35) is an autosomal recessive disorder characterized by brain malformations that result in developmental delay, oculomotor apraxia, and hypotonia. Some patients have renal and retinal involvement (Alkanderi et al., 2018). For a discussion of genetic heterogeneity of Joubert syndrome, see JBTS1 (213300). [from OMIM]

Available tests

8 tests are in the database for this condition.

Clinical tests (8 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: ARFL3, JBTS35, RP83, ARL3
    Summary: ADP ribosylation factor like GTPase 3

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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