Dystrophy na akan tantanin ido. Rarrabuwa, magani hanyoyin

Macular degeneration ne pathological aiwatar da cewa sau da yawa results a cikin asarar hangen nesa. Lokacin da akwai lalacewar da degeneration na sel da intercellular abu, wanda ya haddasa wani canji na jikin ayyuka.

Macular degeneration ne classified a kan da dama filaye.

1. By irin rayuwa cuta. Rarrabe ruwa, ma'adinai, mai, da furotin da kuma carbohydrate.
2. A wuri na alama. Rarrabe cell, gauraye da extracellular.
3. Ruwan dare. Rarrabe tsakanin tsari da kuma gida.
4. By asalin (etiology). Rarrabe nakasar da samu.

Marasa lafiya koka matalauta da hangen nesa, da kuma a duka idanu, takaita cikin filin karkashin review, kusan xari bisa dari makanta a cikin duhu, ba daidai ba launi ji.

Lokacin da akalla daya daga wadannan cututtuka kamata nan da nan nemi sana'a taimako da kuma fara wani hanya na lura.

Macular degeneration ne ya sa ta dalilai da yawa:

- cuta daga cikin jini daga cikin jijiyoyi. Take hakkin da jini ne a precipitating factor a cikin cuta.

- take hakkin Lymph wurare dabam dabam. Kullum, maimaita lymphadenitis.

- cututtuka na jiki (tsofaffi).

- endocrine cuta, hormonal glitch adam bango.

- wani rashin daidaituwa a cikin tafiyar matakai na rayuwa da kwayoyin, cin cuta Kwayoyin manyan zuwa degeneration.

Don takaice, zamu iya cewa shi ne m jini wurare dabam dabam, kafa salon salula nama, shi ne babban dalilin degeneration na akan tantanin ido.

Macular degeneration sau da yawa rinjayar mazan mutane, amma matasa ne kuma batun irin wannan hadarin. Alal misali, wani mutum ya gani a kusa-sightedness. Sakamako ne da karuwa a cikin gangara girma daga ido, sa'an nan mahara karuwa a matsa lamba harsashi, da kuma sakamakon - retinal dystrophy.

Raunin ya sãme ta idanu, musamman a kan su mucous membranes ne mai kowa hanyar retinal degeneration. By guda korau dalilai sun hada da kullum ido cuta, koda cuta, zuciya da jijiyoyin jini tsarin, da sakamako daga dukan nau'i na da gubobi.

Daya nau'i na tsanani hereditary cuta na akan tantanin ido ne myotonic dystrophy. game da zuwa 16 shekaru na farko alamun cutar. A halayyar bayyanar cututtuka na myotonic dystrophy ne tsoka spasms a cikin yatsunsu da taban da ake tsokoki, da tsoka atrophy, yafi fuska da wuya. Haƙuri nablyudetsya hanci pronunciation sauti saboda da atrophy na bulbar tsokoki, da hašari mai cutarwa, numfashi canji. Rashin lafiya ba rikitarwa da idanu, da endocrine tsarin. Bisa kididdigar da, shi ya zama m, 1 daga 8 dubu, da kuma maza sau uku fiye da sau da yawa. A magani ne sosai rare, fiye da na kowa m.

Jiyya dystrophy na akan tantanin ido da ake sa dangane da asibiti hoto da cutar da kuma irin dystrophy. A kusan dukkan lokuta, symptomatic magani (da nufin magance bayyanar cututtuka da cutar), saboda yawancin cutar ne hereditary.

A lura da retinal dystrophy likita ance kawai dace Hanyar ga wani ba haƙuri. A halin yanzu aikata ra'ayin mazan jiya hanyoyin, Laser kuma m.

Kamar yadda amfani disaggregants magani, magunguna, fadada cikin jini, anti-sclerotic shirye-shirye (tsofaffi da marasa lafiya), a hade da bitamin, biogenic stimulators.

Tasiri ne amfani da jiki far: electrophoresis (ba tare da wani-shpoy, gepatrinom), a low-makamashi Laser ruri.

Kintace a hereditary siffofin degeneration na akan tantanin ido m kawo karshen makanta.