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Tessadori-Van Haaften neurodevelopmental syndrome 4

Summary

Tessadori-Bicknell-van Haaften neurodevelopmental syndrome-4 (TEBIVANED4) is characterized by global developmental delay with poor overall growth, variably impaired intellectual development, learning difficulties, distal skeletal anomalies, and dysmorphic facies. Some patients have visual or hearing deficits. The severity and manifestations of the disorder are highly variable (Tessadori et al., 2022). For a discussion of genetic heterogeneity of TEBIVANED, see TEBIVANED1 (619758). [from OMIM]

Genes See tests for all associated and related genes

  • Also known as: H4-16, H4/m, H4C1, H4C11, H4C12, H4C13, H4C14, H4C15, H4C16, H4C2, H4C3, H4C4, H4C5, H4C6, H4C8, H4FM, H4M, HIST1H4I, TEBIVANED4, TEVANED4, H4C9
    Summary: H4 clustered histone 9

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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