Fagadau W R, Heinemann M H, Cotlier E
Int Ophthalmol. 1981 Aug;4(1-2):113-22. doi: 10.1007/BF00139585.
The Hermansky-Pudlak Syndrome, a "tyrosinase positive' form of oculocutaneous albinism, is a triad comprising albinism, a hemorrhagic diathesis and ceroid-lipofuscin storage. A pedigree is presented showing consanguinity with a pattern of pseudodominance. Electroretinography in two isolated Hermansky-Pudlak subjects was distinctly abnormal, showing decreased rod and cone responses (as well as abnormal flicker fusion responses) in one patient, and reduced photopic and scotopic responses in another. The decreased ERG responses are discussed with reference to the known retinal abnormalities in both generalized oculocutaneous albinism and Batten's disease, another ceroid-lipofuscin storage disorder.
赫尔曼斯基-普德拉克综合征是一种“酪氨酸酶阳性”的眼皮肤白化病,是一种三联征,包括白化病、出血素质和类蜡样脂褐质沉积。本文展示了一个具有假显性模式的近亲结婚谱系。对两名孤立的赫尔曼斯基-普德拉克综合征患者进行的视网膜电图检查明显异常,一名患者显示视杆和视锥反应降低(以及异常的闪烁融合反应),另一名患者的明视觉和暗视觉反应降低。本文参照全身性眼皮肤白化病和另一种类蜡样脂褐质沉积病——巴滕病中已知的视网膜异常情况,对视网膜电图反应降低进行了讨论。