Oliver McFarlane Syndrome: A 25‐year follow‐up
- 30 September 1989
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 34 (2) , 199-201
- https://doi.org/10.1002/ajmg.1320340213
Abstract
We describe findings in a 29‐year‐old woman with Oliver McFarlane syndrome after 25 years of follow‐up, and we review findings in six other reported cases. Pigmentary retinal degeneration, trichomegaly, prenatal onset growth failure, anterior pituitary deficiencies, and peripheral neuropathy characterize the condition.Keywords
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