Anotia is the severe form of microtia anomalies that involve pinna and external auditory canal present at birth is rare to be associated with congenital facial nerve palsy. The author reports a man with Right side Anotia and ipsilateral facial nerve palsy. This is rare report of such an association in adult patient had right Anotia and ipsilateral right facial palsy
Otocephaly is a condition characterized by aplasia or hypoplasia of mandible, a small oral fissure a...
Salivary gland choristoma is an extremely rare middle ear mass and is hypothesized to be caused by s...
Background: Microtia is a congenital defect characterized by disturbances in the size and form of th...
Congenital Aural Atresia (CAA) is the failure of development of the external auditory canal. It usua...
Copyright: © 2013 Singh et al., This is an open access article published under the terms of the Cre...
Objectives The aim of this study was to analyze the incidence of inner ear anomalies in patients wit...
AbstractBoth duplication anomalies and external auditory canal stenosis can result in cholesteatoma ...
Cervico-aural [collaural fistula] fistula is rare and it accounts for less than 5% of branchial clef...
Otocephaly is a rare lethal neurocristopathy of first branchial arch, characterized by agnathia (age...
Otocephaly is a condition characterized by aplasia or hypoplasia of mandible, a small oral fissure a...
First branchial cleft anomalies (FBCA) such as duplication of the external auditory canal are due to...
We report a 4 month old female infant, 3rd in order of birth of the first cousin consanguineous pare...
Facial paralysis in a newborn is called congenital facial paralysis (CFP). The major role of the phy...
Background: Microtia is a congenital defect characterized by disturbances in the size and form of th...
Background: Microtia is a congenital defect characterized by disturbances in the size and form of th...
Otocephaly is a condition characterized by aplasia or hypoplasia of mandible, a small oral fissure a...
Salivary gland choristoma is an extremely rare middle ear mass and is hypothesized to be caused by s...
Background: Microtia is a congenital defect characterized by disturbances in the size and form of th...
Congenital Aural Atresia (CAA) is the failure of development of the external auditory canal. It usua...
Copyright: © 2013 Singh et al., This is an open access article published under the terms of the Cre...
Objectives The aim of this study was to analyze the incidence of inner ear anomalies in patients wit...
AbstractBoth duplication anomalies and external auditory canal stenosis can result in cholesteatoma ...
Cervico-aural [collaural fistula] fistula is rare and it accounts for less than 5% of branchial clef...
Otocephaly is a rare lethal neurocristopathy of first branchial arch, characterized by agnathia (age...
Otocephaly is a condition characterized by aplasia or hypoplasia of mandible, a small oral fissure a...
First branchial cleft anomalies (FBCA) such as duplication of the external auditory canal are due to...
We report a 4 month old female infant, 3rd in order of birth of the first cousin consanguineous pare...
Facial paralysis in a newborn is called congenital facial paralysis (CFP). The major role of the phy...
Background: Microtia is a congenital defect characterized by disturbances in the size and form of th...
Background: Microtia is a congenital defect characterized by disturbances in the size and form of th...
Otocephaly is a condition characterized by aplasia or hypoplasia of mandible, a small oral fissure a...
Salivary gland choristoma is an extremely rare middle ear mass and is hypothesized to be caused by s...
Background: Microtia is a congenital defect characterized by disturbances in the size and form of th...