Phenylketonuria mwa ana

Nthawi zina malingaliro abwino ndi chiyembekezo chomwe amachititsa kuti makolo achichepere akhale ochepa akhoza kuchoka mu gulu limodzi. Mwachitsanzo, matenda oopsa ndi phenylketonuria.

Zifukwa za phenylketonuria mwa ana

Phenylketonuria ndi matenda a chibadwa, chomwe chimakhala chophwanya amino acid metabolism, kutanthauza kuti kulibe kwa puloteni phenylalanine hydroxylase, yomwe imayambitsa kusinthanitsa kwa phenylalanine, mapuloteni omwe amapezeka mu zakudya zambiri zomwe zimadya chakudya. Osagawanika mapuloteni ndi ngozi yaikulu ku ubongo wa munthu ndi manjenje.

Matendawa sali osowa kwambiri - m'mabuku okwana 7,000. Mwamwayi, mwana yemwe ali ndi matendawa amatha kuwonekera mwa makolo omwe ali ndi thanzi labwino, pokhapokha ngati onsewo akunyamula geni la "sleeping" la phenylketonuria.

Zizindikiro za phenylketonuria

Vuto la matenda ndiloti n'zosatheka kuzizindikira pa nthawi ya khanda popanda mayesero apadera. Ndipo zizindikiro zoyamba zikhoza kuwonekera mu miyezi 2-6 okha:

Ngati matendawa sakuwululira nthawi ndipo sakuyamba mankhwala, kuchepetsa maganizo kumatha kufika pamtunda waukulu.

Phenylketonuria: Kuwunika

Kuti azindikire nthawi yake, matendawa akugwiritsidwa ntchito - kufufuza magazi a mwana wakhanda kuti akhale ndi phenylalanine. Ngati zizindikirozo zikukweza, mwanayo amatumizidwira kwa geneticist kuti afotokoze za matendawa.

Phenylketonuria: mankhwala

Chinthu chachikulu mwa chithandizo cha matenda oopsa awa ndi zakudya zabwino ndi phenylketonuria. Chofunika kwambiri cha zakudya m'kutulutsidwa kwa mankhwala omwe ali ndi phenylalanine, ndiko kuti, zakudya zonse zamapuloteni. Kuperewera kwa mapuloteni kudzadzaza ndi mapangidwe apadera a amino acid.

Ndili ndi zaka, mphamvu ya mitsempha ya puloteni imatha kuchepa ndipo pafupifupi odwala onse omwe ali ndi phenylketonuria atatha zaka 12 mpaka 14 amasinthana ndi chakudya choyenera.