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Ring chromosome 2 in a child with growth failure and few congenital abnormalities

✍ Scribed by Vigfusson, Norman V. ;Kapstafer, Kennard J. ;Lloyd, Marilyn A. ;Optiz, John M.

Publisher: John Wiley and Sons
Year: 1980
Tongue: English
Weight: 361 KB
Volume: 7
Category: Article
ISSN: 0148-7299
DOI: 10.1002/ajmg.1320070321

No coin nor oath required. For personal study only.

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## Abstract Ring chromosome 21 syndrome is a rare condition with a well‐characterized phenotype. Affected individuals have recognizable dysmorphic features, developmental delays, growth retardation, and a predisposition for congenital malformations involving the neurologic, craniofacial, digestive,