"Antley-Bixler syndrome (ABS), also known as trapezoidocephaly-synostosis syndrome, is a rare autosomal dominant or recessive condition characterised by craniosynostosis and extra-cranial synostoses. Mid-facial hypoplasia is also common."
"Mutations in two separate genes FGFR2 and POR have been found to produce the Antley-Bixler syndrome phenotype."
"FGFR2 is inherited in an autosomal dominant manner and POR is in an autosomal recessive manner."
"History and etymology"