DYSTROPHIA RETICULARIS LAMINAE PIGMENTOSAE RETINAE
DYSTROPHIA RETICULARIS LAMINAE PIGMENTOSAE RETINAE
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网状营养不良症
DOI:
10.1111/j.1755-3768.1950.tb05361.x
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发表时间:
1950
影响因子:
3.4
通讯作者:
H. Sjögren
中科院分区:
文献类型:
--
作者:
H. Sjögren
2.”) Bodihl A. Age 8. Presented with myopia the first time on Sept. 23, 1946. Right eye: Sclera immediately outside limbus corresponding to the upper temporal circumference of the cornea, was markedly thin with the choroid showing through, slightly bulging forward; best described as beginning intercalary staphyloma. The anterior chamber was extremely shallow, almost absent in the peripheral portions. In the pupillary area only a narrow slit remained of the chamber. The pupil was of about normal size, slightly elongated upwards nasally. The pupillary reactions were normal. The iris tissue was of normal appearance. On diascleral transillumination the pigmented layer a t the temporal portion of the base of the iris was found to be markedly atrophic. After dilatation of the pupil by means of homatropine, the lens was laid bare, only the upper nasal portion still being covered by the iris. The lens border was distinctly rounded so that the lens was almost globular. The zonular fibres were clearly visible. The optic disc was normal. There was no dislocation of the vessels which were normal also in other respects. In the centre of the fovea was seen a black spot which on high magnification was found to consist of an accumulation of fine pigment-granules; the fovea was otherwise normal. The macular reflexes were normal. A clearly defined network of black pigmented lines was noticed over the area between the temporal vessels. (Fig. 1). The meshes were formed from sharp