Judisch G F, Lowry R B, Hanson J W, McGillivary B C
Arch Ophthalmol. 1981 Feb;99(2):253-6. doi: 10.1001/archopht.1981.03930010255006.
Four reports of a rare syndrome characterized by severe, early-onset chorioretinopathy, trichosis, and evidence of pituitary dysfunction are reviewed. Recently obtained follow-up information about these four patients is presented. A new example of this disease, the fifth case to be reported, to our knowledge, is described.
