De novo 10q22 interstitial deletion

Lola Cook, David D. Weaver, James K. Hartsfield, Gail H. Vance

Research output: Contribution to journalArticle

9 Scopus citations

Abstract

We describe a 4 month old male with a de novo interstitial deletion of chromosome 10q22. His clinical features included growth deficiency, developmental delay, ocular hypertelorism, posteriorly rotated ears, retrognathia, and fifth finger clinodactyly. He later developed dental lamina cysts of the alveolar ridge. To our knowledge, this is the first reported case of an interstitial deletion of 10q22.

Original languageEnglish (US)
Pages (from-to)71-72
Number of pages2
JournalJournal of Medical Genetics
Volume36
Issue number1
StatePublished - Mar 9 1999

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Keywords

  • Chromosome 10
  • Deletion 10q
  • Interstitial deletion
  • Multiple congenital anomaly (MCA) syndrome

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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