Article
Clinical phenotype associated with terminal 2q37 deletion.
Clinical genetics - 1 Sept 1995
Conrad B, Dewald G, Christensen E, Lopez M, Higgins J, Pierpont M E
Abstract excerpt
Three children with deletions of the terminal portion of the long arm of chromosome 2 [del (2) (q37)] are described and their clinical findings compared to published cases of 2q terminal deletions. Common clinical findings include development delay, macrocephaly, frontal bossing, depressed nasal bridge and cardiac anomaly. Hypotonia and repetitive behavior are also seen during different times of development. The...
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