ʻO Phenylketonuria i nā keiki

I kekahi manawa,ʻo nā'ōnaeho maikaʻi a me nā manaolana e hoʻohuli i nā mākua i hiki ke hele i waho i kahi neʻe. ʻO kekahi laʻana, he hōʻailona weliweliʻo phenylketonuria.

Nā kumu o phenylketonuria i loko o nā keiki

ʻO ka Phenylketonuria he maʻi aʻi, ke kumu o ia ka hōʻinoʻana i keʻano o ka amino acid metabolism,ʻo ia hoʻi, ka nele o ka enzyme phenylalanine hydroxylase,ʻo ia ka mea e pono ai ke kūʻaiʻana i phenylalanine, ka mea i loaʻa i ka hapanui o nā meaʻai i kaʻai. ʻAʻole ka'āpana puʻupuʻu i kahi pilikia nui i ka lolo a me ke kino o nā mea.

ʻAʻole i laha ka maʻi - i ka 1 o 7000 mau hihia. ʻO ka mea pōʻino, hiki i kahi keiki me kēia maʻi ke hōʻike i nā mākua olakino maikaʻi,ʻoiaiʻo lāua ka mea e lawe ana i ka latent, "gene" gene of phenylketonuria.

Nā hōʻailona o phenylketonuria

ʻO ka pilikia o kēia maʻi he mea hikiʻole ke hoʻomaopopo i ka wā o ke keiki hānau me ka hoʻoholoʻoleʻana i nā hoʻokolohua. A hiki i nā hōʻailona mua ke hōʻike waleʻia i ka 2-6 mahina:

Ināʻaʻole i hōʻikeʻia ka maʻi ma ka manawa aʻaʻole e hoʻomauʻia, hiki i ka loiloi manaʻo ke hiki i kahi kiʻekiʻe.

Phenylketonuria: Nānā

No kaʻike kūpono o ka maʻi, ua hoʻohanaʻia ka nānāʻana i ka neonatal - kahi haʻawina o ke koko o kahi keiki hānau e komo i loko o phenylalanine. Inā hōʻoia nā mea hōʻailona, ​​hoʻounaʻia ke keiki i kahi geneticist e hoʻomākāka i kaʻike.

ʻO Phenylketonuria: hana

ʻO ka mea nui i loko o ka hōʻailona o kēia maʻiʻino eʻai pono me ka phenylketonuria. ʻO ke kumu o kaʻaiʻana ma ka hoʻohanaʻoleʻana i nā huahana i loaʻa i loko o ka phenylalanine,ʻo ia hoʻi, nā meaʻai a pau o ka pilina o nā holoholona. E hoʻopihaʻia ka paʻakikī o ka protein i nā huihuhu amino acid nui.

Me ka makahiki, ua emi iho ka noʻonoʻo o ka pūʻali o ka pūpū i ka momona o ka mea nonpote a me nā mea maʻi a pau loa me phenylketonuria ma hope o 12-14 makahiki ke hele i kahiʻai maʻamau.