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Accessory tragus

Known as: Pretragal Duplication, Preauricular tags, Preauricular tag 
Variably shaped, cartilage-containing tissue anterior to the external auditory meatus. [eom:095679c21044c851]
National Institutes of Health

Related topics

Related topics

15 relations
Acrocallosal SyndromeBRANCHIOOTIC SYNDROME 3 (disorder)Burn-Mckeown syndromeCat eye syndrome

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2003
2003
Mosaicism del(8p)/inv dup(8p) in a dysmorphic female infant: a mosaic formed by a meiotic error at the 8p OR gene and an independent terminal deletion event
Various chromosomal rearrangements are associated with the distal 8p region. Among them are the inv dup(8p),1 del(8p22),2–5 and… 
2003
2003
Molecular characterization of a unique de novo 15q deletion associated with Prader–Willi syndrome and central visual impairment
We report a 2‐year‐old boy with Prader–Willi Syndrome (PWS) caused by a deletion of the PWS critical region as a result of an… 
1994
1994
Face lift without preauricular scars.
A subperiosteal rhytidectomy is described that corrects aging of the forehead, the orbital region, the nasolabial fold, and the… 
Review
1993
Review
1993
Bilateral accessory tragus.
Bilateral accessory tragus is a rare congenital malformation of the external ear. An isolated, nonfamilial occurrence of… 
Review
1989
Review
1989
The accessory tragus--no ordinary skin tag.
An accessory tragus can easily be treated by surgical excision. The results are quite satisfactory if care is taken to remove any… 
Highly Cited
1988
Highly Cited
1988
Multiple congenital anomaly/mental retardation (MCA/MR) syndrome with Goldenhar complex due to a terminal del(22q).
We present a case of terminal del(22q) with Goldenhar complex including hemifacial microsomia, bilateral epibulbar dermoids… 
1981
1981
The aetiology of the cat eye syndrome reconsidered.
The cat eye syndrome (CES), usually ascribed to the presence of a deleted supernumerary 22 chromosome, is characterised by a… 
Review
1975
Review
1975
Trisomy 22. Two new cases and delineation of the phenotype.
Two unrelated children, not affected with Down's syndrome, with strikingly similar phenotypes and an extra G-like chromosome are… 
Review
1974
Review
1974
Inheritance of branchial sinuses and preauricular fistulae.
On the basis of two families in which branchial sinus and pre-auricular fistulas occurred together, and a review of the… 
Highly Cited
1971
Highly Cited
1971
The 4p- syndrome. A clinically recognizable chromosomal deletion syndrome.
Partial deletion of the short arm of chromosome 4 results in a clinically recognizable and distinct syndrome. Common features… 
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