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Oliver McFarlane syndrome: a 25-year follow-up
J R Sampson1, J L Tolmie, J S Cant
1Duncan Guthrie Institute of Medical Genetics, University of Glasgow, Scotland.
American Journal of Medical Genetics
|October 1, 1989
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.