Hereditary maʻi - cystic fibrosis: na symptoms a me ka hoikeana o ka maʻi

Cystic fibrosis mea he hereditary maʻi , kena ae la ia e ka mutated'ōewe ua wehewehe aku ma lesions o na pancreas, luna 'iaea ooieoeiiaeuiiai kāna hana o ka ÷ naehana hanu nā loko, a me ka gastrointestinal'āpana.
Ma ka naau o ka cystic fibrosis maʻi, konaʻike, ua i ma ka kakahiaka nui elemakule mea he aaiaoe mutation. I ka maʻi i loko o ia lŘlŘ kekahi keiki o elua tausani, wale e pili ana i ka hapakolu o nā hihia make ma mua o ka makahiki o ke kanakolu. Inā ua hōʻike 'nā mākua o ka mutated'ōewe, o ka pilikia o ka loaa i ke keiki me ka maʻi piʻina i 25%. Nō kāu, nā moku halihali mokulele'āno'ē'ōewe 'aʻole e hana eha iaʻi mai ka cystic fibrosis.

Ma nā pēpē i ka poe i diagnosed me cystic fibrosis symptoms i ke kakahiaka nui lā. About ke kolu i hanau he mea meconium ileus, kūpono ma blockage o ka distal māhele o ka liilii, liʻiliʻi (viscosity) a me ka mānoanoa meconium. Ma ka lua o ka lā ma hope o ka hanau ana o ka maʻi keiki i restless, ka mea ana bloating, ka luaʻi paha regurgitation o ka memo. A mau lā ma hope o ka keiki ka ke ano worsens aie i ka mea ulu o ka intoxication. I ka wā o ka hoʻomaka iaʻi complications o meconium peritonitis a me intestinal perforation.
No hoi, aia no he paakiki cough, aʻe 'o ka noho, keiki lag ma ke kua i loko o ka physical pelane - pau keia kumu no cystic fibrosis. e lanakila Symptoms ma kekahi i kekahi. No ka laʻana, ka mea cough ua i hookuu i ke ano o ke keena naehana'āpana maʻiʻaʻai hou pili. Ma ka hoʻomaka ia mea maloʻo a me ka pohihihi, alaila progresses a lilo maʻi. E like me ka hopena, me ka puʻu fits hoʻomaka e hoʻonāukiuki ka luaʻi.

E hoomanawanui i ka poe i hoopakele cystic fibrosis, symptoms mea he pinepine copious ino-kekahi 'noho, a me ka maʻiʻo o undigested ai i koe. Fecal paʻakikī, e holoiʻia ia, mai ka cradle a me ka ipu hao, i ke alo o ka hiki impurities o hiki momona. Kekahi hoʻomanawanui iki mai i ka haule ana mai o ka rectum.
I ka 70 pakeneka o ka hihia i ka maʻi me ka nānā 'ia ma ka 2 makahiki mua o ke ola. I kamaliʻi makahiki i ka 'ike o cystic fibrosis me ka mehana ano o ka mutation, a me ka malama ana o ka pancreas pili. Ma adulthood, na hihia o cystic fibrosis maʻi, na symptoms hiki ke loaʻa loa kākaʻikahi, wale ma atypical lapaʻau hihia.

I kēia lā, e pakele no ka anomaly mea,ʻaʻole hiki. Hoʻomanawanui iki mai i kaʻike, o cystic fibrosis hana maikaʻiʻole ma luna o ka papa 'aelike ke hōʻoia i ka piha loa ola. A me ka koke ia kaʻike, ua i, lapaʻau ua hoʻomaka ', i ka mea i oi aku ke kumu i ka hoʻomanawanui, e e maikaʻi. E hana 'ia i loko o ka lapaau ana i ka maʻi i alakai aku ai i nā hualoaʻa e ae na wahine me kaʻike, weliweli, e hiki ka hanau keiki elemakule. Kamaʻilioʻana, e hoomahuahua i ka ola kōmi.
Nā mea maʻi me ka cystic fibrosis i ko lakou wa e ola ana ka pono i ka nui nā māhele, e lawe ka lapaʻauʻia e pepehi i ka mucus, a i 'ole ma ke kaʻawaleʻana. No ka ulu a me ka ulu ana o na keiki hoʻomaka i kaʻawaʻawaʻana hoomakaukau, ai ole i ka ai, e hou e ke kemu. Ua Radio he nui kūlana maikai no kou kino. I ka mana i ka maʻiʻaʻai ana i ka ÷ naehana hanu'ōnaehana, no ke kokua a me ka Kāohiʻana o relapse pono antibiotics. Inā au i cystic fibrosis, ua kaheaia symptoms o a ma ke akepaʻa lesions, hepatic pono regularʻai ana, i hoonui ae i ka hana o ke ake keena, a lahilahi i ke koko.

I ka lapaʻau Ua koi 'ia e like me ka kekahiʻai, ua hoomahuahua ia ka maʻiʻo o ka a dala o ke kumuʻiʻo, mea momona a me ka carbohydrate loaʻa nui e hoʻopili like i ka makahiki. Hoonohoia nā wikamina. Maʻi keiki e mau ia ma lalo o ka hooponopono ana o ke kauka. Inā i ka maʻi, aole ia e holomua, hospitalization ua i koi 'ia. Ma ke kīhāpai o ka maʻi keiki, 'aʻole pono e kipaku, i ke kula i hoʻonohonoho' ia i ka kūikawā? Eia no ia.