The boy sees apples " L One changes two " R It is a rare hereditary disease not to be near-sighted

The boy sees apples " L One changes two " R It is a rare hereditary disease not to be near-sighted
An article, hope to turn into two at one glance - -Recently, the ophthalmology department of affiliated hospital of Southeast China University accepts such a small patient for medical treatment, not only eyes have ghost images to see objects, finger and toe bone are also much more slender than the ordinary person.
10 -year-old Li Shuang (Assumed name ) On grade three in primary school, parents find Li pair often like narrowing eyes, especially have a class and can not always think claiming clear, a fuzzy slice word on the blackboard.
Mother passes him an apple in once, unexpectedly he regards as two, will also tell mother innocently sometimes, " L How look from distant place you I, come up two mums! " R Li Shuang's parents thought the son suffered from near-sighted eyes, took advantage of bringing him to the hospital to examine on summer vacation.
Check, find Li pair move at the serious lens, structure at all different with the intersection of normal child and eyeball carefully. Ophthalmology department Zhang Rui doctor analyze patient move at the serious lens, light that object reflect become one picture, fetching light to be systematic to become first picture inside eyeball in lens. Because of forming picture two times, Li Shuang's eyes will see objects one is turned into two.
Through check, make a definite diagnosis of, the all (Marfan) on horse trouble Syndrome, this is a kind of inborn, dominant genetic disease of the autosome, also let the crystal malposition point syndrome long, the clinical symptom skeleton muscle system is shown as slender four limbs, the upper part of the body is half-lengther and longer than to leave, long head deformity, surface are narrow, muscles are undeveloped, the skin is low in tension. The intersection of eye and symptom show as crystal dislocate or half dislocation, high myopia, cataract, retinal stripping, iris tremble etc..
It is introduced, all the syndrome patient, with the deformity of inborn cardiovascular vessels of horse of 80%, easy to initiate dying suddenly. This disease is comparatively rare, the incidence is less than 1/10000.
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