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Related Experiment Video

Updated: Nov 24, 2025

Author Spotlight: Three-Dimensional Cephalometric Landmark Annotation Demonstration on Human Cone Beam Computed Tomography Scans
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Author Spotlight: Three-Dimensional Cephalometric Landmark Annotation Demonstration on Human Cone Beam Computed Tomography Scans

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Facial cleft syndrome--a case report.

S M Betharia1, S Kumar

  • 1Dr. R.P. Centre for Ophthalmic Science, A.I.I.M.S., New Delhi.

Indian Journal of Ophthalmology
|October 1, 1990
PubMed
Summary

This report details a rare facio-orbital anomaly involving a dermolipoma and corpus callosum lipoma. Surgical management and classification of facial cleft deformities are discussed.

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Articles linked to this work by shared authors, journal, and citation graph.

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Same author

Prognostic relevance of serum hyaluronan levels in patients with breast cancer.

International journal of cancer·1992
Same author

Acceptability trials with ready to eat foods in a rural area.

Indian pediatrics·1992
Same author

American Diabetes Association annual scientific sessions, San Antonio, 20-23 June 1992.

Diabetic medicine : a journal of the British Diabetic Association·1992
Same author

Localization of the gene for branchiootorenal syndrome to chromosome 8q.

Genomics·1992
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Expression of DRG during murine embryonic development.

Biochemical and biophysical research communications·1992
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DRG: a novel developmentally regulated GTP-binding protein.

Biochemical and biophysical research communications·1992

Area of Science:

  • Ophthalmology
  • Plastic Surgery
  • Neurology

Background:

  • Facial cleft deformities represent a spectrum of congenital anomalies requiring precise classification and tailored surgical approaches.
  • Dermolipomas are benign choristomas often presenting with orbital involvement, necessitating careful evaluation of associated structures.

Observation:

  • A rare case of facio-orbital anomaly is presented, characterized by a dermolipoma with posterior extension.
  • Associated findings include a lid notch, ectropion, asymmetric hypertelorism, and an incidental lipoma of the corpus callosum.

Findings:

  • The case highlights the complex interplay of congenital anomalies affecting the face and orbit.
  • Comprehensive diagnostic imaging is crucial for identifying all components of such rare syndromes.

Implications:

  • This case underscores the importance of a multidisciplinary approach in managing complex craniofacial and orbital malformations.
  • Understanding the classification and surgical nuances of facial cleft deformities is vital for achieving optimal functional and aesthetic outcomes.

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