Primary hyperoxaluria type 1-a rare hereditary metabolic disorder as cause of livedo racemosa
© 2023. The Author(s), under exclusive licence to Springer Medizin Verlag GmbH, ein Teil von Springer Nature..
Livedo racemosa is characterized by a bizarrely configurated lightning figure-like appearance with striated to reticulated, livid erythematous macules and results from a reduced perfusion of the respective skin area, which can have different underlying pathophysiologies. A rare but relevant cause, especially in young patients with end-stage kidney failure, is primary hyperoxaluria type 1 (PH1), a hereditary metabolic disorder in which oxalate accumulates in the body.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2024 |
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| Erschienen: |
2024 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:75 |
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| Enthalten in: |
Dermatologie (Heidelberg, Germany) - 75(2024), 4 vom: 23. März, Seite 321-324 |
| Sprache: |
Deutsch |
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| Weiterer Titel: |
Primäre Hyperoxalurie Typ 1 – eine seltene hereditäre Stoffwechselstörung als Ursache einer Livedo racemosa |
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| Beteiligte Personen: |
Linse, Kai-Philipp [VerfasserIn] |
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| Links: |
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| Themen: |
Cutaneous oxalosis |
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| Anmerkungen: |
Date Completed 27.03.2024 Date Revised 27.03.2024 published: Print-Electronic Citation Status MEDLINE |
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| doi: |
10.1007/s00105-023-05276-6 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| 520 | |a Livedo racemosa is characterized by a bizarrely configurated lightning figure-like appearance with striated to reticulated, livid erythematous macules and results from a reduced perfusion of the respective skin area, which can have different underlying pathophysiologies. A rare but relevant cause, especially in young patients with end-stage kidney failure, is primary hyperoxaluria type 1 (PH1), a hereditary metabolic disorder in which oxalate accumulates in the body | ||
| 650 | 4 | |a English Abstract | |
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| 650 | 4 | |a Kidney failure | |
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