Bosun I
Clinica Oftalmologică, Craiova.
Oftalmologia. 1996 Apr-Jun;40(2):129-35.
The analysis of twenty-one observations with Peter Syndrome, shows that the disease was established by a disorder in the development of the mesoderm who gives birth at the posterior, stratum of cornea, iris stroma and angle of the posterior chamber. The disease was associated with cataract (nine cases), strabismus (seven cases), congenital glaucoma (five cases), microophthalmia (three cases), microcornea (four cases), remainders of the pupillary membrane (one case), vitreous opacities (one case), facial malformations (one case), congenital dacryocystitis (one case), nystagmus (four cases). The presence at the same patient of the posterior keratoconus or staphiloma of cornea at one eye and Peter syndromme at the other eye, is possible to say that these diseases are evolutionary stages by one and the same mesodermal disgenesia.
对21例彼得综合征患者的分析表明，该疾病是由中胚层发育紊乱引起的，中胚层发育异常导致角膜后层、虹膜基质和后房角的形成。该疾病与白内障（9例）、斜视（7例）、先天性青光眼（5例）、小眼症（3例）、小角膜（4例）、瞳孔膜残留（1例）、玻璃体混浊（1例）、面部畸形（1例）、先天性泪囊炎（1例）、眼球震颤（4例）有关。同一患者一只眼睛出现后圆锥角膜或角膜葡萄肿，另一只眼睛患有彼得综合征，可以说这些疾病是同一中胚层发育不全的不同演变阶段。
