See Also: acrocephalosyndactyly type 1(medicine)
type V acrocephalosyndactyly(medicine)
type IV acrocephalosyndactyly(medicine)
type III acrocephalosyndactyly(medicine)
type I acrocephalosyndactyly(medicine)
type II acrocephalosyndactyly(medicine)
Herbal medicine (botanical medicine, herbology, phytomedicine)(health)
acrocephalosyndactyly(medicine)
Acrocephalosyndactyly(health)
Apert syndrome acrocephalosyndactyly(health)

type III acrocephalosyndactyly (medicine)


type III acrocephalosyndactyly


An autosomal dominant syndrome with variable expression of brachycephaly, maxillary hypoplasia, prominent ear crus, syndactyly, facial asymmetry, shallow orbits, telecanthus, and nasal septal deviation; may show mental retardation.

Synonym: Saethre-Chotzen syndrome.