De novo 10q22 interstitial deletion

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

Research output: Contribution to journalArticle

9 Citations (Scopus)

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
Pages (from-to)71-72
Number of pages2
JournalJournal of Medical Genetics
Volume36
Issue number1
StatePublished - 1999

Fingerprint

Retrognathia
Hypertelorism
Alveolar Process
Chromosome Deletion
Fingers
Ear
Cysts
Tooth
Growth

Keywords

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

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

De novo 10q22 interstitial deletion. / Cook, Lola; Weaver, David; Hartsfield, James K.; Vance, Gail.

In: Journal of Medical Genetics, Vol. 36, No. 1, 1999, p. 71-72.

Research output: Contribution to journalArticle

Cook, L, Weaver, D, Hartsfield, JK & Vance, G 1999, 'De novo 10q22 interstitial deletion', Journal of Medical Genetics, vol. 36, no. 1, pp. 71-72.
Cook, Lola ; Weaver, David ; Hartsfield, James K. ; Vance, Gail. / De novo 10q22 interstitial deletion. In: Journal of Medical Genetics. 1999 ; Vol. 36, No. 1. pp. 71-72.
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