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undergraduate thesis
LIJEČENJE RANE FAZE MIŠIĆNE DISTROFIJE
2019. urn:nbn:hr:150:377446
Laptoš, Martina
University of Applied Sciences "Lavoslav Ružička" in Vukovar
Department for Medical Studies

Cite this document

Laptoš, M. (2019). LIJEČENJE RANE FAZE MIŠIĆNE DISTROFIJE (Undergraduate thesis). Vukovar: University of Applied Sciences "Lavoslav Ružička" in Vukovar. Retrieved from https://urn.nsk.hr/urn:nbn:hr:150:377446

Laptoš, Martina. "LIJEČENJE RANE FAZE MIŠIĆNE DISTROFIJE." Undergraduate thesis, University of Applied Sciences "Lavoslav Ružička" in Vukovar, 2019. https://urn.nsk.hr/urn:nbn:hr:150:377446

Laptoš, Martina. "LIJEČENJE RANE FAZE MIŠIĆNE DISTROFIJE." Undergraduate thesis, University of Applied Sciences "Lavoslav Ružička" in Vukovar, 2019. https://urn.nsk.hr/urn:nbn:hr:150:377446

Laptoš, M. (2019). 'LIJEČENJE RANE FAZE MIŠIĆNE DISTROFIJE', Undergraduate thesis, University of Applied Sciences "Lavoslav Ružička" in Vukovar, accessed 20 March 2025, https://urn.nsk.hr/urn:nbn:hr:150:377446

Laptoš M. LIJEČENJE RANE FAZE MIŠIĆNE DISTROFIJE [Undergraduate thesis]. Vukovar: University of Applied Sciences "Lavoslav Ružička" in Vukovar; 2019 [cited 2025 March 20] Available at: https://urn.nsk.hr/urn:nbn:hr:150:377446

M. Laptoš, "LIJEČENJE RANE FAZE MIŠIĆNE DISTROFIJE", Undergraduate thesis, University of Applied Sciences "Lavoslav Ružička" in Vukovar, Vukovar, 2019. Available at: https://urn.nsk.hr/urn:nbn:hr:150:377446

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Metadata
TitleLIJEČENJE RANE FAZE MIŠIĆNE DISTROFIJE
Title (english)TREATMENT OF EARLY-STAGE MUSCULAR DYSTROPHY
AuthorMartina Laptoš
MentorSlavica Janković (mentor)
Committee memberGordana Bujišić (predsjednik povjerenstva)
Committee memberSlavica Janković (član povjerenstva)
Committee memberDražen Pejić (član povjerenstva)
GranterUniversity of Applied Sciences "Lavoslav Ružička" in Vukovar
(Department for Medical Studies)
Vukovar
Defense date and country2019-09-26, Croatia
Scientific / art field,
discipline and subdiscipline		BIOMEDICINE AND HEALTHCARE
Clinical Medical Sciences
Abstract
Mišićne distrofije nasljedne su bolesti karakterizirane progresivnom mišićnom slabosti i atrofijom mišića. Pripadaju skupini neuromišićnih bolesti koje obuhvaćaju nasljedne i stečene bolesti perifernog neuromišićnog sustava, uključujući zahvaćenost stanica prednjih rogova kralježnične moždine, perifernih živaca, neuromišićnih spojeva i mišića. Različiti oblici variraju prema kliničkoj slici, brzini progresije kliničke slike, patološkim promjenama mišića, prema načinu nasljeđivanja i dobi... More pojavnosti simptoma. Duchenneova mišićna distrofija (DMD) najčešća je dječja mišićna distrofija koja zahvaća dječake. Pojava bolesti počinje se očitovati oko treće godine života. Prvi simptomi vezani su uz hod, a uzrok tome je simetrična slabost mišića zdjeličnog i ramenog obruča. Slabost mišića uzrokuje sporije kretnje, otežano provođenje aktivnosti koje zahtijevaju zajedničko usklađeno djelovanje grupa mišića kao što je penjanje uz stepenice, ustajanje s poda, podizanje stvari iznad glave i slično. Prisutan je hod na prstima, geganje, pozitivan Gowersov znak, povećana lumbalna lordoza i pseudohipetrofija mišića potkoljenice. Slabost se postepeno širi s donjih na gornje ekstremitete, vrat i respiratorne mišiće. Cilj je ovog rada prikazati Duchenneovu mišićnu distrofiju te njezino liječenje s posebnim naglaskom na liječenje rane faze samostalnog hoda. Liječenje rane faze podrazumijeva održavanje snage u proksimalnim mišićima ekstremiteta, tj.zdjeličnog i ramenog pojasa, sprječavanje ili usporavanje daljnjeg gubitka mišićne snage i održavanje snage u mišićima koji su bitni za održavanje ravnoteže. Less
Abstract (english)
Muscular dystrophies are hereditary diseases that are characterized by progressive muscle weakness and muscle atrophy. They belong to a group of neuromuscular diseases which include hereditary and acquired diseases of the peripheral neuromuscular system including involvement of the cells of the anterior horns of the spinal cord, peripheral nerves, neuromuscular junctions and muscles. The different forms vary according to the clinical picture, the rate of progression of the clinical... More picture, the pathological changes of the muscles, the mode of inheritance and the age of onset of symptoms. Duchenne muscular dystrophy (DMD) is the most common childhood muscular dystrophy affecting boys. The disease itself begins to manifest around the age of three. The first symptoms are related to gait, and the cause is symmetrical muscle weakness of the pelvic and shoulder hoops. The muscle weakness causes slower movements, difficulty performing activities that require joint action by muscle groups such as climbing stairs, getting up from the floor, lifting things overhead etc. Finger gait, gagging, Gowers’ sign, increased lumbar lordosis, and pseudohypertrophy of the lower leg muscles are present. The weakness gradually spreads from the lower to the upper extremities, neck, and respiratory muscles. The aim of this paper is to present Duchenne muscular dystrophy and its treatment with special emphasis on the treatment of the early stage of independent walking. Early stage treatment involves maintaining strength in the proximal extremity muscles, i.e. the pelvic and shoulder girdles, preventing or slowing further loss of muscle strength, and maintaining strength in the muscles that are essential for maintaining balance. Less
Keywords
Keywords (english)
Languagecroatian
URN:NBNurn:nbn:hr:150:377446
Study programmeTitle: Physiotherapy
Study programme type: professional
Study level: undergraduate
Academic / professional title: stručni/a prvostupnik/prvostupnica (baccalaureus/baccalaurea) fizioterapije (stručni/a prvostupnik/prvostupnica (baccalaureus/baccalaurea) fizioterapije)
Type of resourceText
File originBorn digital
Access conditionsAccess restricted to students and staff of home institution
Terms of useLicence In copyright icon
Created on2019-09-30 07:10:04
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