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Case Reports
. 1980 Dec;17(6):480-3.
doi: 10.1136/jmg.17.6.480.

Craniosynostosis and syndactyly: expanding the 11q-- chromosomal deletion phenotype

B M Lippe, R S Sparkes, B Fass, L Neidengard
Case Reports

Craniosynostosis and syndactyly: expanding the 11q-- chromosomal deletion phenotype

B M Lippe et al. J Med Genet. 1980 Dec.

Abstract

A patient with a partial deletion (q23 leads to qter) of the long arm of chromosome 11 presented with craniosynostosis and syndactyly. These characteristics, which have not been previously reported with 11q--, expand the phenotype of this syndrome and emphasise the need for chromosome analysis with banding techniques in multiple congenital anomaly syndromes, even if the patient could be classified as having a non-chromosomal syndrome.

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References

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