Short report
De novo 10q22 interstitial deletion
Lola Cooka, David D Weavera, James K Hartsfield Jra c, Gail H Vancea b
a Division
of Clinical Genetics, Department of Medical and Molecular Genetics,
Indiana University School of Medicine, 975 West Walnut Street,
Indianapolis, IN 46202-5251, USA, b Division of Cytogenetics, Department of Medical
and Molecular Genetics, Indiana University School of Medicine,
Indianapolis, IN, USA, c Department of Oral-Facial Development, Indiana
University School of Dentistry, Indianapolis, IN, USA
Correspondence to: Ms Cook.
Received 30 October
1997;
Revised version accepted for publication 20 May 1998
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.
Keywords: chromosome 10; interstitial deletion; deletion 10q; multiple congenital anomaly (MCA) syndrome
© 1999 by J Med Genet
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