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GTR Home > Conditions/Phenotypes > Lethal congenital contracture syndrome 6

Lethal congenital contracture syndrome 6

Summary

Lethal congenital contracture syndrome-6 (LCCS6) is an autosomal recessive disorder characterized by multiple flexion and extension contractures resulting from lack of fetal movements, severe polyhydramnios, and absent stomach (Patel et al., 2014). For a general phenotypic description and a discussion of genetic heterogeneity of LCCS, see LCCS1 (253310). [from OMIM]

Available tests

17 tests are in the database for this condition.

Clinical tests (17 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: LCCS6, ZNF925, ZBTB42
    Summary: zinc finger and BTB domain containing 42

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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