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A bifid nose (also known as cleft nose) is an uncommon congenital malformation which is characterized by the presence of a cleft between the two nostrils of the nose. [1] It is the result of a disturbance during embryological nose development. [2] It is part of the Tessier classification for craniofacial clefts. [3]
Nasal deformity correction: The correction of the broad nasal base is simultaneously done with the orbital hypertelorism repair. This is for good alignment of the eyes with the nose for the best aesthetic result. A bifid nose tip will only be treated at the age of 18, when the patient's skeleton has fully matured. [7] [21]
Frontonasal dysplasia (FND) is a congenital malformation of the midface. [1] For the diagnosis of FND, a patient should present at least two of the following characteristics: hypertelorism (an increased distance between the eyes), a wide nasal root, vertical midline cleft of the nose and/or upper lip, cleft of the wings of the nose, malformed nasal tip, encephalocele (an opening of the skull ...
as a haemostat; replace tonsil artery forceps; ligature will not slip due to curve tip. St. Clair Thompson adenoid curette with cage and guard: used in adenoid surgery.held in dagger holding fashion and passed behind soft palate. Yankauer's nasopharyngoscope: for a direct access or look at the nasopharynx: Yankauer suction tip
muscle hook or squint hook; sharp tip or knobbed tip; used in squint surgery Foreign body spud and needle: Spud to remove superficial and needle for the deep foreign bodies in the eye Elliot's trephine with handle: used in corneal donation (eye donation) to cut out the cornea in a circular fashion Castroveijo's calipers: various measurements ...
These clefts bisect the face vertically through the midline. Tessier number 0 bisects the maxilla and the nose, Tessier number 14 comes between the nose and the frontal bone. The Tessier number 30 facial cleft is through the tongue, lower lip and mandible. The tongue may be absent, hypoplastic, bifid, or even duplicated. [5]
Trigonocephaly-bifid nose-acral anomalies syndrome is a very rare genetic disorder which is characterized by trigono brachycephaly, narrow forehead, up-ward slanting palpebral fissures, bulbous, slightly bifid nose, macrostomia, thin upper lip, macrognathia (facial dysmorphisms), broad thumbs, rather large toes, broad fingertips with short nail beds, joint hypermobility and fifth finger ...
Because the nose is the anchor-feature of the face, an aesthetically proportionate nose balances the physiognomic features of a person. Non-surgical correction is considered for patients with a treatment-suitable aesthetic defect, or a defect resulting from a surgical rhinoplasty (either primary or secondary).