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GTR Home > Conditions/Phenotypes > Craniosynostosis and dental anomalies

Craniosynostosis and dental anomalies

Synonyms
KREIBORG-PAKISTANI SYNDROME
Modes of inheritance
Autosomal recessive inheritance (Orphanet)

Summary

CRSDA is an autosomal recessive disorder characterized by craniosynostosis, maxillary hypoplasia, and dental anomalies, including malocclusion, delayed and ectopic tooth eruption, and/or supernumerary teeth. Some patients also display minor digit anomalies, such as syndactyly and/or clinodactyly (summary by Nieminen et al., 2011). [from OMIM]

Available tests

20 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (20 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CRSDA, IL11RA
    Summary: interleukin 11 receptor subunit alpha

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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