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Widow's peak

Known as: Hairline peak, Hairline point, V-shaped frontal hairline 
Frontal hairline with bilateral arcs to a low point in the midline of the forehead. [pmid:19125436]
National Institutes of Health

Related topics

Related topics

12 relations
Aarskog syndromeAcrofacial dysostosis Catania formAutosomal dominant inheritanceCraniofrontonasal dysplasia

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
A STUDY OF SOME MORPHOGENETIC TRAITS AMONG THE ESAN ETHNIC GROUP OF NIGERIA.
BACKGROUND Genetic variability is a common feature of many organisms. The existence of genetic variation in man is caused by many… 
2013
2013
Endoscope-assisted submandibular sialoadenectomy via retroauricular hairline approach: Anatomical study
Objective To provide the anatomical basis for the endoscope-assisted submandibular sialoadenectomy via retroauricular hairline… 
2010
2010
The Scent of Cancer
If forced to choose, I would give up the sense of smell first. It is both the hardest sense to take for granted and the easiest… 
Review
2008
Review
2008
Avoiding the operated on look in multiple face lifts.
Review
2006
Review
2006
Atrioventricular block and wiry hair in Teebi hypertelorism syndrome
We report on a 4½‐year‐old girl with clinical features of Teebi hypertelorism syndrome (THS), including a prominent forehead with… 
2005
2005
New dental findings in the median cleft facial syndrome.
BACKGROUND The main features of median cleft facial syndrome are hypertelorism, cranium bifidum occultum, widow's peak, and… 
2001
2001
Syndrome of short stature, widow's peak, ptosis, posteriorly angulated ears, and joint problems: exclusion of the Aarskog (FGD1) gene as a candidate gene.
A syndrome encompassing postnatal onset of short stature, widow's peak, ptosis, posteriorly angulated ears, and limitation of… 
1999
1999
Prenatal sonographic diagnosis of Aarskog syndrome.
In 1970, Aarskog described a rare X‐linked developmental disorder characterized by short stature in association with a variety of… 
1995
1995
Teebi hypertelorism syndrome: further observations.
A new autosomal dominant syndrome resembling craniofrontonasal syndrome was identified by Teebi [1987: Am J Med Genet 28:581-591… 
1977
1977
THE 7p PARTIAL TRISOMY SYNDROME
Various partial trisomy syndromes have been described since the advent of the chromosome banding techniques. However, a… 
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