Ukuthola i-muscular dystrophy diagnostic enembile ingenye yezinselelo isimo esikunikezayo. Ngokuvamile, i-dystrophy ye-muscular ibangelwa ukungabi khona noma ukungasebenzi kwamaprotheni okuthiwa i-dystrophin, esebenza ngokudala ibhuloho emkhatsini wezintambo zakho zomzimba kanye nendawo ezungezile, okusiza ukudlulisa iziphambano zakho ze-muscular ezindaweni ezikude.
Uma le phrotheni ingasebenzi kahle noma ingekho, ukulahleka kwemisipha nokubuthakathaka kwenzeka. Ukuhlola le phrotheni, phakathi kwezinye izivivinyo, kusiza ngokufanele ukuxilonga i-muscular dystrophy.
Ukuhlaziywa kwezimpawu nakho kusiza ukuhlukanisa phakathi kwezinhlobo eziyisishiyagalolunye zezinyosi ze-muscular dystrophy. Bahlukaniswa ngethulo lomtholampilo wabo.
Ukuhlola Ukuzihlola Nekhaya
Ukuxilongwa kokuqala kwe-muscular dystrophy kuvame ukukwenziwa uma kuqala izimpawu. Ukubona ukuthi umzimba wakho usebenza kanjani-nokuguqula-kungakuholela ekumangaliseni i-dystrophy yemisipha.
I-dystrophy muscular dystrophy , uhlobo oluvame kakhulu, lunezici ezithile zezimpawu eziholela abantu ekuphethweni ukuthi bangaba nesifo. Lezi zimpawu zingabandakanya:
- Ubuthakathaka bemisipha ezungeze isikhumba sakho, izinqulu, nemilenze, okwenza kube nzima ukuhamba nokulawula i-trunk.
- Ubusha. I-dystrophy yama-muscular iyakuthinta kakhulu izingane, ikakhulukazi uhlobo lwe-Duchenne noma lwe-Becker.
- Kunzima ukuma nokuhamba.
- Ukungahlali okungahleliwe noma okudlula.
- Ukuhlushwa nokuwa phansi.
Uma unesinye salezi zimpawu, kubalulekile ukuthi uvakashele udokotela wakho ngokushesha. Ungakwazi ukuhlola ukuhlolwa komtholampilo nokuhlola ukuqinisekisa noma ukulawula ukukhishwa kwamathambo okuphuma ngaphandle kwemisipha bese uqala ukwelashwa okungcono kwesimo sakho.
I-dystrophy yama-musculaza isifo sofuzo futhi sizuze njengefa lomunye wabazali bakho. Umlando womndeni walesi sifo uyisici sokuthi lesi sifo sibangela izimpawu zakho.
Ama-Labs nezivivinyo
Uma udokotela wakho esebenzile ukuhlolwa komtholampilo wobuthakathaka bakho bemisipha, angase ahlele ukuhlolwa okukhethekile ukuqinisekisa ukuthi ukuxilongwa. Lokhu kungafaka:
- Ukuhlolwa kwegazi. Ama-enzyme acacisiwe akhululwa egazini lapho kunesisindo sokuchitha. La ma-enzyme, okuthiwa i-serum creatine kinase kanye ne-serum aldolase, angase abonise ukuthi ukulahleka kwemisipha kwenzeka ngenxa yokudonswa kwemisipha.
- Ukuhlolwa kofuzo. Njengoba i-dystrophy ye-muscular iyimvelo, ukuhlolwa kwezakhi zofuzo kungenziwa kuwe nabazali bakho ukunquma ukuthi i-dystrophin yegene ethile ikhona yini kwi-X yakho ye-chromosome. Lokhu kungaqinisekisa ukuxilongwa kwe-dystrophy ye-muscular.
- Ukuhlolwa kwamandla. Ukuhlolwa kwamandla usebenzisa i-dynamometer kunganikeza ukulinganisa okunembile kwamandla akho futhi kungaholela udokotela wakho ukuqinisekisa ukuthi i-dystrophy ye-muscular.
- I-muscle biopsy. I-biopsy ye-muscle iyisivivinyo lapho ingxenye encane yemisipha yakho isuswe futhi ihlolwe ngaphansi kwe-microscope. Ukuhlolwa kungabonisa ulwazi mayelana nezakhi zofuzo ezithile kanye namaprotheni abangela i-muscular dystrophy, okuholela ekuxilongweni.
- Ukuhlolwa kwezinhliziyo. Ngezinye izikhathi, i-dystrophy yemisipha ingathinta izicubu zenhliziyo. Ukuhlolwa kwe-cardiac kungenziwa ukuze kunqume ukuthi inhliziyo yakho iyathinteka yini ngesimo sakho.
- Ukuhlolwa kwe-Electromyogram (EMG) . Ukuhlolwa kwe-EMG kwenziwa ukukala umsebenzi we-muscle. Ukunciphisa umsebenzi we-muscle kungabonisa i-dystrophy yama-muscular.
Ngokuvamile, ukuxilongwa kwe-muscular dystrophy akukwenziwe ngokuhlolwa okulodwa noma isilinganiso; kunalokho ukuhlolwa okuningi futhi isethulo sakho semitholampilo sisetshenziselwa ukuhlonza kahle isimo sakho.
Ukucabanga
Nakuba ukuxilongwa kwe-muscular dystrophy ngokuyinhloko kwenziwa ngokuhlolwa komtholampilo, ukuhlolwa kofuzo, nokuhlolwa kwegazi, udokotela wakho angase acele ukuhlolwa kwe-imagination magnetic resonance (MRI) .
Lokhu kusetshenziselwa ukuhlola ubuningi bezinsizi nezicubu. Ngokuvamile njengoba imisipha ilahlekile, ithathelwa izicubu ezinamafutha; i-MRI ingasetshenziswa ukuhlola lokhu.
Ukuhlonza okuhlukile
Ngisho noma unobuthakathaka emzimbeni wakho (noma endaweni eyodwa yomzimba wakho), akusho ukuthi une-dystrophy yemisipha. Ezinye izimo zingase zibangele ubuthakathaka bomzimba. Lokhu kungafaka:
- Isimo somlomo wesibeletho noma se-lumbar. Lokhu kubuthakathaka obangelwa ukucindezelwa kwesibindi se-peripheral emgodleni wakho.
- Izimo zezinzwa. Ezinye izimo ze-neuromuscular zingabangela ubuthakathaka. Lezi zingabandakanya i- multiple sclerosis (MS) noma i- amyotrophic lateral sclerosis (ALS) .
- Ubuthakathaka obangelwa yimithi. Eminye imiphumela emibi yemithi ingabangela ubuhlungu besisu nokubuthakathaka. Udokotela wakho kanye nosokhemisi angasiza ekunqumeni ukuthi lokhu kubangela ubuthakathaka bakho.
Uma uzizwa noma yiluphi uhlobo lwesisu esingavamile noma ukukhubazeka, kufanele ubone udokotela wakho ngaso leso sikhathi. Angenza ukuhlolwa okuphelele futhi asebenze noma aphume ukuxilongwa kwe-muscular dystrophy. Ngaleyo ndlela, ungaqala ukwelashwa okungcono kwesimo sakho.
> Umthombo:
> Korschun, H. (2007, Julayi 3). Ukuthola nokuxilongwa kwe-dystrophy yemisipha kuqhutshelwa ukuhlolwa okusha kwezakhi zofuzo. Izindaba zezokwelapha namuhla. Ibuyiselwe ngoJuni 21, 2012, kusukela ku-http: //www.medicalnewstoday.com/releases/75515.php