RT Journal Article
SR Electronic
T1 De novo 10q22 interstitial deletion
JF Journal of Medical Genetics
JO J Med Genet
FD BMJ Publishing Group Ltd
SP 71
OP 72
DO 10.1136/jmg.36.1.71
VO 36
IS 1
A1 Cook, Lola
A1 Weaver, David D
A1 Hartsfield, James K
A1 Vance, Gail H
YR 1999
UL http://jmg.bmj.com/content/36/1/71.abstract
AB 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.