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Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1989 Jul;26(7):470–472. doi: 10.1136/jmg.26.7.470

Unknown syndrome: Noonan-like craniofacial features, digital anomalies, and premature birth.

R C Shepherd 1, D R Goudie 1, J L Tolmie 1
PMCID: PMC1015655  PMID: 2746622

Abstract

We report a mother and two of her children, one female and the other male, who have ptosis, hypertelorism, epicanthic folds, downward slanting palpebral fissures, broad nasal bridge, and minor digital anomalies (fig 1); the children had delayed closure of a large anterior fontanelle. All three affected persons were born prematurely.

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Selected References

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