'Apert syndrome' presentation slideshows

Hereditary diseases. Congenital malformations.

1.14k views • 96 slides

Craniofacial and Pharyngeal Arch Development

Craniofacial and Pharyngeal Arch Development. Matthew Velkey matt.velkey@duke.edu 454D Davison. Two general phases of pharyngeal apparatus development. Wk 3.5. Wk 4.5. Wk 5.5. Wk 6.5. Disruptions to either phase can result in a broad spectrum of defects.

2.03k views • 44 slides

SOCIAL TRANSFORMATION OF AMERICAN MEDICINE

SOCIAL TRANSFORMATION OF AMERICAN MEDICINE. MEDICAL EDUCATION WAS RETARDED MUTUAL HOSTILITY INTENSE COMPETETION DIFFERNCE IN ECONOMIC INTEREST SECTARIAN ANTAGONISM. KING MINOS. Daedalus Icarus. CRANIOSTENOSIS CRANIOSYNOSTOSIS CRANIOFACIAL ANOMALIES.

382 views • 24 slides

APERT SYNDROME

APERT SYNDROME. BY Milana Abayev DEN2311/D246 11/26/15. Apert syndrom. It is a rare type I genetic disorder characterized by premature fusion of skull ( craniosynostosis). It affects the normal growth of head and face and also extremities such as fused figures and toes (syndactyly).

431 views • 12 slides

Apert Syndrome

Apert Syndrome. What is Apert Syndrome?. Apert syndrome is a genetic disorder in which the fingers, face, toes, or feet are mutated. Apert syndrome can be inherited from a parent who has it or through a genetic mutation.

3.81k views • 9 slides

Apert Syndrome

Apert Syndrome. By: Alex M. Discovered. Apert Syndrome was discovered in 1906 by a French Physician named Eugene Apert. Apert diagnosed nine patients which all experienced the following symptoms. Symptoms .

908 views • 7 slides