Definición:
Craniostenosis characterized by acrocephaly and syndactyly, probably occurring as an autosomal dominant trait and usually as a new mutation. (Dorland, 27th ed)
Sinónimos:
Sindrome de Apert /
SÃndrome de Apert /
SÃndrome de Saethre-Chotzen /
Sindrome de Saethre-Chotzen /