Search results
Results from the WOW.Com Content Network
Microtia is a congenital deformity where the auricle (external ear) is underdeveloped. A completely undeveloped auricle is referred to as anotia . Because microtia and anotia have the same origin, it can be referred to as microtia-anotia . [ 1 ]
Microtia Freudenthal, 1976 (preoccupied) Mikrotia is an extinct rodent belonging to the Muridae . It lived during the upper Miocene (about 11.63 - 5 million years ago) and its fossil remains have been found in Italy ( Gargano ).
Microtia is a monophyletic genus of butterflies from southern United States and Central America in the family Nymphalidae. It contains the single species Microtia elva , the elf . [ 1 ] Larvae of this species feed on Tetramerium and other species in the family Acanthaceae .
The search engine that helps you find exactly what you're looking for. Find the most relevant information, video, images, and answers from all across the Web.
Burt Brent is a retired reconstructive plastic surgeon best known for his work in reconstructing the absent outer ear. He built upon the techniques of his mentor, Dr. Radford Tanzer [1] of the Mary Hitchcock Clinic at Dartmouth Medical School and repaired ear defects in 1,800 patients, most of them children born with ear deformities such as microtia.
Pierre Robin sequence [a] (/ p j ɛər r ɔː ˈ b æ̃ /; [3] abbreviated PRS) is a congenital defect observed in humans which is characterized by facial abnormalities.The three main features are micrognathia (abnormally small mandible), which causes glossoptosis (downwardly displaced or retracted tongue), which in turn causes breathing problems due to obstruction of the upper airway.
Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!
Molecular genetic Testing determines that FGF3 is the only gene whose mutation can cause congenital deafness with Michel aplasia, microdontia and microtia. Carrier testing for at-risk relatives requires identification of mutations which are responsible for occurrence of disease in the family.