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Goldenhar Syndrome

Known as: Facial Dysplasias, Lateral, Hemifacial Microsomia, Disease, Goldenhar 
A congenital birth defect characterized by incomplete development or absence of face structures, usually affecting one side of the face. The defects… 
National Institutes of Health

Related topics

Related topics

11 relations

Narrower (1)

Axial mesodermal dysplasia spectrum
Congenital Systemic DisorderFaceGoldenhar Syndrome with Ipsilateral Radial DefectHemifacial microsomia

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2010
2010
A rare variation in the course of the inferior alveolar nerve.
Highly Cited
2008
Highly Cited
2008
A human papillomavirus-associated disease with disseminated warts, depressed cell-mediated immunity, primary lymphedema, and anogenital dysplasia: WILD syndrome.
BACKGROUND Epidermodysplasia verruciformis (EV) is a rare genodermatosis associated with infections with specific human… 
Review
2007
Review
2007
Bone anchored hearing aid in children--prevention of complications.
Highly Cited
2006
Highly Cited
2006
Congenital absence of the portal vein in oculoauriculovertebral dysplasia (Goldenhar syndrome)
Absence of the portal vein with systemic visceral venous return was demonstrated in an 8-year old girl with… 
Review
1999
Review
1999
Hemifacial microsomia and treatment options for auricular replacement: A review of the literature.
Review
1990
Review
1990
Pigmentary dysplasias, hypomelanosis of Ito, and genetic mosaicism.
  • D. Flannery
  • American journal of medical genetics
  • 1990
  • Corpus ID: 43326318
This editorial reviews and synthesizes a perspective on current knowledge regarding pigmentary dysplasias and genetic admixtures… 
1977
1977
The Goldenhar syndrome: a natural history.
: Twenty-four patients with the 1st branchial arch (Goldenhar) syndrome have been ascertained ranging in age from newborn to 58… 
1975
1975
Lateral facial dysplasia (first and second branchial arch syndrome, hemifacial microsomia).
Highly Cited
1964
Highly Cited
1964
WAARDENBURG'S SYNDROME AND HETEROCHROMIA IRIDUM IN A DEAF SCHOOL POPULATION.
  • M. Partington
  • Canadian Medical Association journal
  • 1964
  • Corpus ID: 45127013
Waardenburg's syndrome consists of lateral displacement of the inner canthi of the eyes (dystopia canthorum), a broad nasal root… 
1960
1960
Craniofacial dysostosis, patent ductus arteriosus, hypertrichosis, hypoplasia of labia majora, dental and eye anomalies-a new syndrome?
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