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It is called preauricular sinus which, according to the U.S. National Institutes of Health, or NIH, "generally appears as a tiny skin-lined hole or pit, often just in front of the upper ear where ...
The difference between them is that a cyst does not connect with the skin, but a sinus does. [3] Frequency of preauricular sinus differs depending the population: 0.1–0.9% in the US, 0.9% in the UK, and 4–10% in Asia and parts of Africa. [4] Preauricular sinuses are inherited features, and frequently appear next to both ears. [5]
Once her doctor recommended sinus surgery, and insurance confirmed prior authorization wasn't needed, Christine Knirk focused on getting the procedure and getting better. The outpatient operation ...
Nasal surgery is a specialty including the removal of nasal obstruction that cannot be achieved by medication and nasal reconstruction. Currently, it comprises four approaches, namely rhinoplasty, septoplasty, sinus surgery, and turbinoplasty, targeted at different sections of the nasal cavity in the order of their external to internal positions.
Bilateral branchial cleft sinuses during surgery. Four branchial clefts (also called "grooves") form during the development of a human embryo. The first cleft normally develops into the external auditory canal, [8] but the remaining three arches are obliterated and have no persistent structures in normal development. Persistence or abnormal ...
Surgery for cholesteatoma offers the most advantages for using the endoscope instead of the microscope. Failures in cholesteatoma surgery are most common in certain areas of the anatomy of the tympanic cavity, such as the facial recess, sinus tympani, anterior attic, and the protympanum which are poorly accessed with the microscope. [12]
Branchial fistula may need surgery [3] Branchio-oto-renal syndrome (BOR) [ 4 ] [ 5 ] is an autosomal dominant genetic disorder involving the kidneys , ears, and neck. It is also known as Melnick-Fraser syndrome.
Otofaciocervical syndrome, also known as Fara Chlupackova syndrome, [1] are a small group of rare developmental disorders of genetic origin which are characterized by facial dysmorphisms, long neck, preauricular and/or branchial pits, cervical muscle hypoplasia, hearing loss, and mild intellectual disabilities.