Ukufumana i-muscular dystrophy diagnostic echanekileyo ngenye yemingeni imeko. Ngokuqhelekileyo, i-dystrophy ye-muscular ibangelwa ukungabikho okanye ukungasebenzi kweprotheni ebizwa ngokuthi i-dystrophin, esebenza ngokudala ibhuloho phakathi kweemfucu zakho ze-muscle kunye nommandla ojikelezayo, ekuncediseni ukudlulisa izicathulo zakho ze-muscular kwiindawo ezikufutshane.
Xa le prothini ayisebenzi kakuhle okanye ingekho, ukutshabalalisa imisipha kunye nobuthathaka kwenzeka. Ukuvavanywa kule protheni, phakathi kwezinye iimvavanyo, kunceda ngokufanelekileyo ukuxilonga i-muscular dystrophy.
Uhlalutyo lweempawu lukunceda ukuhlula phakathi kweentlobo ezi-9 ezahlukeneyo ze-muscular dystrophy. Ziyahlukana ngokweentetho zabo zekliniki.
Ukuvavanya nokuzihlola kwekhaya
Ukuxilongwa kokuqala kwe-muscular dystrophy ngokuqhelekileyo kwenziwa xa kuvela iimpawu. Ukuqwalasela indlela umzimba wakho osebenza ngayo-kunye nokutshintsha-kunokukhokelela ekukrokrezeni i-dysstrophy ye-muscular.
I-duchenne muscular dystrophy , uhlobo oluqhelekileyo, luneempawu ezibonakalayo ezikhokelela abantu kwisigqibo sokuba banokuba nesifo. Ezi zimpawu zingabandakanya:
- Ububuthakathaka beemisipha zijikeleze i-pelvis yakho, iminyango, nemilenze, obangela ubunzima ngokuhamba kunye nokulawula i-trunk.
- Ubutsha. I-muscular dysstrophy ichaphazela abantwana, ingakumbi uhlobo lweDuchenne okanye lwe-Becker.
- Ukuma kunzima nokuhamba.
- Ukungaqiniseki okanye ukukhawuleza.
- Ukuhlutha kunye nokuwa phantsi.
Ukuba unayo nayiphi na le mpawu, kubalulekile ukuba u tyelele ugqirha wakho ngokukhawuleza. Unako ukwenza uvavanyo lwekliniki kunye nokuvavanya ukuqinisekisa-okanye ukulawula i-dysstrophy ngaphandle kwe-muscular kwaye uqalise kunyango olungcono kwiimeko zakho.
I-muscular dysstrophy isifo sofuzo kunye nefa elivela kubazali bakho. Imbali yentsapho yalo mqathango yinkcazelo yokuba isifo sibangela iimpawu zakho.
IiLabs kunye novavanyo
Emva kokuba ugqirha wakho enze uvavanyo lweklinikhi yobuthakathaka bakho be-muscular, unokuyalela imivavanyo ekhethekileyo ukuqinisekisa ukuxilongwa. Ezi ziquka:
- Ukuhlolwa kwegazi. Ama-enzyme athile akhululwa kwigazi xa kukho ukutshabalaliswa kwemisipha. Ezi enzyme, ezibizwa ngokuthi i-serum creatine kinase kunye ne-serum aldolase, zingasethetha ukuba ukuxhatshazwa kwemisipha kwenzeke ngenxa yesifo se-dystrophy.
- Vavanyo lwe-Genetic. Ekubeni i-dystrophy ye-muscular iyimvelaphi yelifa, ukuhlolwa kofuzo kungenziwa kuwe nabazali bakho ukuchonga ukuba ngaba i-dystrophin yegeni ekhoyo kwi-X yakho ye-chromosome. Oku kungaqinisekisa ukuxilongwa kwe-muscular dysstrophy.
- Ukuvavanywa kwamandla. Ukuvavanywa kwamandla usebenzisa i-dynamometer kunokunika ubungqina obuchanekileyo bamandla akho kwaye kunokukhokelela ugqirha wakho ukuqinisekisa ukunyuka kwesifo se-muscular dystrophy.
- I-biopsy ye-Muscle. I-biopsy ye-muscle iyimvavanyo apho inxalenye encinci yeesisundu sakho seesisu isuswe kwaye ihlolwe phantsi kwe-microscope. Uviwo luyakubonisa ulwazi malunga neejethi ezithile kunye neeprotheyini ezibangelwa i-muscular dysstrophy, ekhokelela ekuxilongweni.
- Vavanyo lwe kliniki. Ngamanye amaxesha, i-muscular dystrophy inokuchaphazela iisisu zomzimba. Uvavanyo lwendiza lunokwenziwa ukuba lunqume ukuba intliziyo yakho ichaphazelekayo yimeko yakho.
- Uvavanyo lwe-Electromyogram (EMG) . Uvavanyo lwe-EMG lwenziwe ukulinganisa umsebenzi we-muscle. Umsebenzi ophantsi we-muscle ungabonisa i-dystrophy yama-muscular.
Ngokuqhelekileyo, ukuxilongwa kwe-muscular dystrophy akukwenziwe ngumvavanyo othile okanye umlinganiselo othile; kunoko ubuninzi beemvavanyo kunye neentetho zakho zeklinikhi zisetyenziselwa ukuxilongwa ngokuchanekileyo kwimeko yakho.
Ukucinga
Nangona ukuxilongwa kwe-muscular dystrophy ngokukodwa kwenziwa ngokuhlolwa kwekliniki, ukuvavanya iimfuyo kunye nokuhlolwa kwegazi, ugqirha wakho unokuyalela ukuhlolwa kwe -imagination magnetic resonance (MRI) .
Oku kusetyenziselwa ukuhlola ubuninzi bomzimba kunye nezicubu. Ngokuqhelekileyo njengoko isisipha siphelile, sithatyathwa ngamathambo enqatha; I-MRI ingasetyenziselwa ukuhlola oku.
Ukuxilongwa ngokungafani
Nangona unobuthathaka emzimbeni wakho (okanye enye indawo yomzimba wakho), akuthethi ukuba unesifo se-dystrophy. Ezinye iimeko zingabangela ubuthathaka bomzimba. Ezi ziquka:
- Umlomo wesibeleko okanye i-lumbar myelopathy. Oku kubuthathaka obangelwa kukunyanzeliswa kwentsholongwane yomhlaba kwintsipho yakho.
- Iimeko zeentsholongwane. Ezinye izimo ze-neuromuscular zingabangela ubuthathaka. Ezi zibandakanya i- multiple sclerosis (MS) okanye i- amyotrophic lateral sclerosis (ALS) .
- Ubuthathaka obubangelwa ngamachiza. Ezinye iziphumo zempembelelo zonyango zingabangela i-muscle aches kunye nobuthathaka. Ugqirha wakho kunye nekhemistiya unokuncedisa ukuba ngaba oku kubangela ubuthathaka.
Ukuba uvakalelwa naluphi na uhlobo lwesifo esingaqhelekanga okanye ukusilela, kufuneka ubone ugqirha wakho ngokukhawuleza. Unako ukuqhuba uviwo olubanzi kunye nokulawula okanye ukuphuma kwisifo se-muscular dystrophy. Ngaloo ndlela, unokuqaliswa kunyango olungcono kwiimeko zakho.
> Umthombo:
> Korschun, H. (2007, Julayi 3). Ukufumanisa nokuxilongwa kwe-muscular dystrophy eqhutywe nguvavanyo olutsha. News Today. Ibuyiswe ngoJuni 21, 2012, ukusuka http://www.medicalnewstoday.com/releases/75515.php