Severe facial clefting, limbic dermoid, hypoplasia of the corpus callosum, and multiple skin appendages: Severe frontofacionasal "dysplasia" or newly recognised syndrome?

L. I. Al-Gazali, A. H. Dawodu, M. Hamada, M. Bakir, D. Bakalinová

Research output: Contribution to journalArticlepeer-review

8 Citations (Scopus)

Abstract

We report on a child with severe midline facial cleft, bilateral cleft lip and palate, telecanthus, S-shaped palpebral fissures, limbic dermoid, midface bypoplasia, hypoplastic corpus callosum, and multiple skin appendages. This case may be an example of severe frontofacionasal "dysplasia" or a newly recognised syndrome.

Original languageEnglish
Pages (from-to)346-347
Number of pages2
JournalAmerican Journal of Medical Genetics - Seminars in Medical Genetics
Volume63
Issue number2
DOIs
Publication statusPublished - May 17 1996

Keywords

  • Cleft lip and palate
  • Facial cleft

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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