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GTR Home > Conditions/Phenotypes > Al-Gazali syndrome

Summary

Al-Gazali syndrome (ALGAZ) is characterized by prenatal growth retardation, skeletal anomalies including joint contractures, camptodactyly, and bilateral talipes equinovarus, small mouth, anterior segment eye anomalies, and early lethality (summary by Ben-Mahmoud et al., 2018). [from OMIM]

Available tests

9 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Genes See tests for all associated and related genes

  • Also known as: ALGAZ, EDSP2, EDSSPD2, SEMDJL1, beta3GalT6, B3GALT6
    Summary: beta-1,3-galactosyltransferase 6

Clinical features

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