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A child with 18q— syndrome and cerebellar astrocytoma

✍ Scribed by Kathleen W. Faulkner; Lewis B. Holmes; Alan Steinfeld; Israel F. Abroms

Book ID
119460339
Publisher
Elsevier Science
Year
1983
Tongue
English
Weight
289 KB
Volume
103
Category
Article
ISSN
1097-6833

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## Abstract The 18q‐ syndrome [MIM #601808] is a terminal deletion of the long arm of chromosome 18. The most common deletion extends from region q21 to qter. We report here a nine‐year‐old boy possessing a simple 18q‐ deletion who had abnormalities of the brain, skull, face, tooth, hair, bone, and