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Preauricular pit

Known as: Preauricular earpits, pits preauricular, Preauricular pits 
Small indentation anterior to the insertion of the ear. [HPO:sdoelken, pmid:19152421]
National Institutes of Health

Related topics

Related topics

19 relations
Acrocephalopolysyndactyly type 2Andersen SyndromeBRANCHIOOTIC SYNDROME 1BRANCHIOOTIC SYNDROME 3 (disorder)

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Microstructure and Mechanical Properties of Spray Formed and Hot Pressed/HeatTreated Al-(20-30 wt%) Mg2Si-2% Cu Alloy
In the present investigation, Al-(20-30%wt) Mg2Si-2Cu alloys were synthesized by spray forming process and further processed by… 
2009
2009
Perforated ray cells in Miconia ternatifolia: a first report for the family Melastomataceae.
Perforated ray cells have been reported in many plant families (e.g., Chalk & Chattaway 1933; McLean & Richardson 1973) but they… 
Review
2007
Review
2007
Cat eye syndrome associated with schizophrenia.
Schizophrenia is a frequent and complex psychiatric disorder. Current neurobiological research in schizophrenia provides a wealth… 
2006
2006
Renal hypoplasia and dysplasia: starting to put the puzzle together.
The human metanephros is the direct precursor of the mature kidney: It begins to form in the fifth gestational week, when… 
Review
1993
Review
1993
Mineral exploration in the Lower Palaeozoic rocks of south-west Cumbria. Part 1, regional surveys
The results of geochemical, geological and geophysical surveys over Lower Palaeozoic rocks in the south-western part of Cumbria… 
1988
1988
A scanning electron microscopic study of crestal pits on human permanent molars.
1987
1987
Association of tetra-amelia, ectodermal dysplasia, hypoplastic lacrimal ducts and sacs opening towards the exterior, peculiar face, and developmental retardation.
A male child with tetra-amelia, hypotrichosis, upward slanting palpebral fissures, lack of lacrimal openings, hypoplastic… 
1985
1985
An autosomal dominant syndrome of characteristic facial appearance, preauricular pits, fifth finger clinodactyly, and tetralogy of Fallot.
This report describes six relatives with a syndrome of mild prenatal-onset growth deficiency, an altered craniofacial appearance… 
1983
1983
[Branchio-oto-renal dysplasia. A hereditary dominant autosomal syndrome with variable expression].
A pedigree of branchio-oto-renal dysplasia (BOR syndrome) is reported. BOR syndrome is an autosomal dominant disorder in which… 
1979
1979
A case of 21q-syndrome with normal SOD-1 activity
SummaryA female infant with del(21)(pter→q22.1-2:) constitution identified by G, Q, and R banding is reported. She had marked… 
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