"type 1: classic Pfeiffer; most individuals have normal intelligence and lifespan. Inherited in an autosomal dominant pattern."
"type 2: includes a cloverleaf skull (Kleeblattschädel); occurs sporadically and has a poor prognosis with severe neurological compromise."
"type 3: includes craniosynostosis and severe proptosis; occurs sporadically and has poor prognosis."
"type 2: includes a cloverleaf skull (Kleeblattschädel); occurs sporadically and has a poor prognosis with severe neurological compromise."
"Pfeiffer syndrome is strongly associated with mutations of the fibroblast growth factor receptor 1 gene (FGFR1) on chromosome 8 or the fibroblast growth factor receptor 2 (FGFR2) gene on chromosome 10."
"type 1: classic Pfeiffer; most individuals have normal intelligence and lifespan. Inherited in an autosomal dominant pattern."
"type 2: includes a cloverleaf skull (Kleeblattschädel); occurs sporadically and has a poor prognosis with severe neurological compromise."
"type 3: includes craniosynostosis and severe proptosis; occurs sporadically and has poor prognosis."
"type 1: classic Pfeiffer; most individuals have normal intelligence and lifespan. Inherited in an autosomal dominant pattern."
"type 2: includes a cloverleaf skull (Kleeblattschädel); occurs sporadically and has a poor prognosis with severe neurological compromise."
"type 3: includes craniosynostosis and severe proptosis; occurs sporadically and has poor prognosis."
"History and etymology"