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Review
. 1989 Aug;26(8):528-32.
doi: 10.1136/jmg.26.8.528.

De novo terminal deletion 7p22.1--pter in a child without craniosynostosis

F Speleman  1 , M Craen, J Leroy
Affiliations
Review

De novo terminal deletion 7p22.1--pter in a child without craniosynostosis

F Speleman et al. J Med Genet. 1989 Aug.

Abstract

A patient with a de novo terminal deletion of the short arm of chromosome 7 (p22.1--pter) is described. Facial dysmorphism, a congenital heart defect, and genital hypoplasia were evident. There were no signs of craniosynostosis. Our observation confirms that deletion of 7p22 is not necessarily associated with craniosynostosis.

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