Oxycephaly

oxycephaly
ks kefli noun a condition in which the skull is shaped into a point with exophthalmos and poor sight ...
oxygen ...

Craniosynostosis (Scaphocephaly) - Trigonocephaly - Oxycephaly - Crouzon syndrome - Craniodiaphyseal dysplasia - Hypertelorism - Macrocephaly - Treacher Collins syndrome - Platybasia
Spine and bony thorax ...

The primary features are an abnormal shape of the skull (called oxycephaly) and underdeveloped or absent bones in the forearm, primarily the radius (which is why the name craniosynostosis-radial aplasia syndrome is sometimes used).

Syndactylic Oxycephaly
Syndactyly Type I with Microcephaly and Mental Retardation
Syndromatic Hepatic Ductular Hypoplasia
Synergistic Necrotizing Fasciitis of the Perineum and Genitalia
Synovectomy for rheumatoid arthritis ...

Congenital malformation in which oxycephaly, brachysyndactyly of hand, and preaxial polydactyly of feet are associated with mental retardation; it is usually inherited as an autosomal recessive trait but there is also a dominant form.

GR-43175, Health Systems, Community, Healthcare Markets, Helium, Holography, Infections, Escherichia coli, Irradiation, Whole-Body, Leu-1 Antigen, Medical Staffs, Musa, Nerve Block, Sympathetic, NSC 102816, Ocular Infections, Bacterial, Oxycephaly, ...

ASC 1, autosomal dominant trait, craniosurgery, craniosynostosis, FGFR2 gene, fibroblast growth factor receptor 2, fibroblast growth factor receptor 2 gene, intellectual disabilities, midface hypoplasia, syndactyly, syndactylic oxycephaly.

See also: Syndactyly, Sclerosis, Mental retardation, Autosomal dominant, Arthritis