The University of Chicago Header Logo

Antley-Bixler Syndrome Phenotype

"Antley-Bixler Syndrome Phenotype" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

expand / collapse MeSH information
An inherited condition characterized by multiple malformations of CARTILAGE and bone including CRANIOSYNOSTOSIS; midface hypoplasia; radiohumeral SYNOSTOSIS; CHOANAL ATRESIA; femoral bowing; neonatal fractures; and multiple joint CONTRACTURES and, occasionally, urogenital, gastrointestinal or cardiac defects. In utero exposure to FLUCONAZOLE, as well as mutations in at least two separate genes are associated with this condition - POR (encoding P450 (cytochrome) oxidoreductase (NADPH-FERRIHEMOPROTEIN REDUCTASE)) and FGFR2 (encoding FIBROBLAST GROWTH FACTOR RECEPTOR 2).


expand / collapse publications
This graph shows the total number of publications written about "Antley-Bixler Syndrome Phenotype" by people in this website by year, and whether "Antley-Bixler Syndrome Phenotype" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
_