AN INSIGHT INTO - HEMIFACIAL MICROSOMIA

Hemifacial microsomia is a common birth defect involving first and second branchial arch derivatives. The phenotype is highly variable. In addition to craniofacial anomalies, there may be cardiac, vertebral, and central nervous system defects. Most cases are sporadic, but there are rare familial cases that exhibit autosomal dominant inheritance.

• Publication year

  2021

• Venue

  International Journal of Advanced Research

• Publication date

  2021-09-30

• Fields of study

  Not labeled

• Identifiers
  DOI 10.21474/ijar01/13475
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar

• No claims are published for this paper.

• No concepts are published for this paper.

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  1994cited by this paper
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  1993cited by this paper
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  1987cited by this paper
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  1987cited by this paper
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  1987cited by this paper
• Familial occurrence of malformations possibly attributable to vascular abnormalities.

  1986cited by this paper
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  1983cited by this paper
• Hemifacial microsomia and variants: pedigree data.

  1983cited by this paper
• Cranial defects in the Goldenhar syndrome.

  1983cited by this paper
• Further evidence for an autosomal dominant form of oculoauriculovertebral dysplasia

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  1982cited by this paper
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  1981cited by this paper
• Goldenhar syndrome and hemifacial microsomia: Observations on three patients

  1980cited by this paper
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• THE SYNDROME OF GOLDENHAR AFFECTING TWO SIBLINGS

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