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Related Experiment Video

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Electroporation of Craniofacial Mesenchyme
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Diprosopus a Rare Craniofacial Malformation.

Mrinal Bhuyan1, Inamul Haque1

  • 1Department of Neurosurgery, Gauhati Medical College and Hospital, Guwahati, Assam, India.

Asian Journal of Neurosurgery
|November 22, 2018
PubMed
Summary

This study details a rare newborn condition called diprosopus, characterized by facial duplication. The case analysis focuses on associated anomalies, clinical challenges, and the infant's outcome.

Keywords:
Diprosopusfacial duplicationneurulation

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Area of Science:

  • Medical Genetics
  • Developmental Biology
  • Pediatric Surgery

Background:

  • Diprosopus is a rare congenital anomaly with facial duplication.
  • It presents with varying degrees of duplication, from partial to complete.
  • Affected infants typically have a single torso and normal limbs.

Observation:

  • A case of diprosopus was admitted to our institute.
  • Detailed analysis of the infant's specific anomalies was performed.
  • Clinical problems encountered during care were documented.

Findings:

  • The case presented unique craniofacial malformations.
  • Management involved addressing complex clinical issues.
  • The outcome of the presented diprosopus case was evaluated.

Implications:

  • Understanding diprosopus aids in diagnosing and managing rare craniofacial malformations.
  • This case contributes to the limited literature on diprosopus.
  • Improved clinical insights can guide future treatment strategies for affected newborns.