Gargoylismの眼所見について

緒言

　Gargoylism （Dysostosis multiplex-Hurler）はかなり稀な先天性疾患であるが，欧米では近来その報告が増加の一途を辿つており，眼科的にも興味あるものと思えるが，本邦報告の8例^{1）2）3）4）5）6）7）}共小児科並に精神科領域よりなされている。私等は最近本症の典型例2例につき眼所見を観察することが出来たので報告する。

Gargoylism are considerably rare congenital disease and are considered as systemic disease which has tetralogy, namely developement disturbance of bone by which peculiar countenance and head-shape, pigmy, motor disturbance of joints and mental weakness are appeared, cor-neal turbidity, and hepatosplenomegalia, and abnormal deposit of glykogen, glykoprotein and mukoprotein in whole tissue.

Two cases, one is 14 months old boy and onother 12 months old girl, which were typical cases habing tetralogy were presented.

First case was reported by Prof. Kitamura in SHONIKA RINSHO 8:196.