Neuropathology I : muscular diseases
© 2022. The Author(s)..
Muscle diseases include hereditary and acquired diseases with clinical manifestation in both childhood and adulthood. The different muscle diseases may have ultrastructural alterations that help us further understand the pathology of the disease. Specific changes in sarcomere structure help to classify a congenital myopathy. The detection of cellular aggregates supports the classification of myositis. Pathologically altered mitochondria, on the other hand, can occur both in genetic mitochondriopathies but also secondarily in acquired muscle diseases like myositis. Ultrastructural analysis of the myocardium is also helpful in the diagnosis of hereditary cardiomyopathies in childhood. This review article highlights the ultrastructural features of different muscle diseases and pathognomonic findings in specific disease groups.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2023 |
---|---|
Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:44 |
---|---|
Enthalten in: |
Pathologie (Heidelberg, Germany) - 44(2023), 2 vom: 19. März, Seite 104-112 |
Sprache: |
Deutsch |
---|
Weiterer Titel: |
Neuropathologie I: Muskuläre Erkrankungen |
---|
Beteiligte Personen: |
Schänzer, Anne [VerfasserIn] |
---|
Links: |
---|
Themen: |
Cardiomyopathy |
---|
Anmerkungen: |
Date Completed 07.03.2023 Date Revised 10.03.2023 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1007/s00292-022-01163-4 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM349717567 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM349717567 | ||
003 | DE-627 | ||
005 | 20231226043305.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231226s2023 xx |||||o 00| ||ger c | ||
024 | 7 | |a 10.1007/s00292-022-01163-4 |2 doi | |
028 | 5 | 2 | |a pubmed24n1165.xml |
035 | |a (DE-627)NLM349717567 | ||
035 | |a (NLM)36459202 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a ger | ||
100 | 1 | |a Schänzer, Anne |e verfasserin |4 aut | |
245 | 1 | 0 | |a Neuropathology I |b muscular diseases |
246 | 3 | 3 | |a Neuropathologie I: Muskuläre Erkrankungen |
264 | 1 | |c 2023 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 07.03.2023 | ||
500 | |a Date Revised 10.03.2023 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a © 2022. The Author(s). | ||
520 | |a Muscle diseases include hereditary and acquired diseases with clinical manifestation in both childhood and adulthood. The different muscle diseases may have ultrastructural alterations that help us further understand the pathology of the disease. Specific changes in sarcomere structure help to classify a congenital myopathy. The detection of cellular aggregates supports the classification of myositis. Pathologically altered mitochondria, on the other hand, can occur both in genetic mitochondriopathies but also secondarily in acquired muscle diseases like myositis. Ultrastructural analysis of the myocardium is also helpful in the diagnosis of hereditary cardiomyopathies in childhood. This review article highlights the ultrastructural features of different muscle diseases and pathognomonic findings in specific disease groups | ||
650 | 4 | |a English Abstract | |
650 | 4 | |a Journal Article | |
650 | 4 | |a Review | |
650 | 4 | |a Cardiomyopathy | |
650 | 4 | |a Electron microscopy | |
650 | 4 | |a Mitochondria | |
650 | 4 | |a Myositis | |
650 | 4 | |a Vacuoles | |
700 | 1 | |a Dittmayer, Carsten |e verfasserin |4 aut | |
700 | 1 | |a Porubsky, Stefan |e verfasserin |4 aut | |
700 | 1 | |a Weis, Joachim |e verfasserin |4 aut | |
700 | 1 | |a Goebel, Hans-Hilmar |e verfasserin |4 aut | |
700 | 1 | |a Stenzel, Werner |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Pathologie (Heidelberg, Germany) |d 2022 |g 44(2023), 2 vom: 19. März, Seite 104-112 |w (DE-627)NLM337237387 |x 2731-7196 |7 nnns |
773 | 1 | 8 | |g volume:44 |g year:2023 |g number:2 |g day:19 |g month:03 |g pages:104-112 |
856 | 4 | 0 | |u http://dx.doi.org/10.1007/s00292-022-01163-4 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 44 |j 2023 |e 2 |b 19 |c 03 |h 104-112 |