Oliver McFarlane Syndrome: A 25‐year follow‐up

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.

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