Satz N, Kronauer C, Steinmann B, Knoblauch M
Schweiz Med Wochenschr. 1985 Mar 2;115(9):304-6.
A case of congenital familial ptosis with simultaneous Ehlers-Danlos syndrome type II is presented. Since coincidence of these two rare hereditary diseases would be unlikely, the ptosis in this case may be a so far undocumented manifestation of EDS.
