Publication:
Acute Renal Failure due to Rhabdomyolysis in a Child with McArdle Disease

dc.authorscopusid36979398000
dc.authorscopusid10642354300
dc.authorscopusid56510123000
dc.authorscopusid6701319607
dc.authorscopusid6505879209
dc.authorscopusid59606045500
dc.contributor.authorDelibaş, A.
dc.contributor.authorBek, K.
dc.contributor.authorEzgü, F.S.
dc.contributor.authorDemircin, G.
dc.contributor.authorOksal, A.
dc.contributor.authorÖner, A.
dc.date.accessioned2020-06-21T15:13:19Z
dc.date.available2020-06-21T15:13:19Z
dc.date.issued2008
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Delibaş] Ali, Department of Pediatric Nephrology, Mersin Üniversitesi, Mersin, Turkey, Çocuk Saǧliǧi ve Hastaliklari Anabilim Dali, Mersin Üniversitesi, Mersin, Turkey; [Bek] Kenan, Department of Pediatric Nephrology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Ezgü] Faith Süheyl, Department of Pediatric Metabolism and Nutrition, Gazi Üniversitesi, Ankara, Ankara, Turkey; [Demircin] Gülay, Department of Pediatric Nephrology, Dr. Sami Ulus Children's Hospital, Ankara, Turkey; [Oksal] Ayşegül, Department of Pathology, Dr. Sami Ulus Children's Hospital, Ankara, Turkey; [Öner] Ayşe, Department of Pediatric Nephrology, Dr. Sami Ulus Children's Hospital, Ankara, Turkeyen_US
dc.description.abstractRhabdomyolysis induced acute renal failure (ARF) is relatively rare in children. We report an 8-year-old boy with McArdle disease and rhabdomyolysis induced ARF after heavy muscle work. Physical examination revealed generalized tenderness on his extremities. Laboratory examinations showed acute renal failure due to myoglobinuria and revealed alanine transaminase 428 U/l, aspartate transaminase 1,400 U/l, blood urea nitrogen 119 mg/dl, creatinin 3.6 mg/dl, uric acid 13 mg/dl, and serum creatinine kinase (CK) 33,766 U/l. Hemodialysis was carried out for ARF. His clinical and laboratory findings improved and became normal in 2 weeks. Enzymatic analysis of the muscle biopsy showed a phosphorylase A level of 129 nmol/s/mg protein (normal: 200-600) and a phosphorylase A+B level of 385 nmol/s/mg protein (normal: 500-1500), which was compatible with glycogenosis type V. As McArdle disease rarely becomes symptomatic and ARF secondary to this condition is very rare, our case represents a rare clinical presentation. © 2007 Springer-Verlag.en_US
dc.identifier.doi10.1007/s00431-007-0591-z
dc.identifier.endpage940en_US
dc.identifier.issn0340-6199
dc.identifier.issn1432-1076
dc.identifier.issue8en_US
dc.identifier.pmid17899190
dc.identifier.scopus2-s2.0-46149088480
dc.identifier.scopusqualityQ1
dc.identifier.startpage939en_US
dc.identifier.urihttps://doi.org/10.1007/s00431-007-0591-z
dc.identifier.urihttps://hdl.handle.net/20.500.12712/19224
dc.identifier.volume167en_US
dc.identifier.wosWOS:000257204200014
dc.identifier.wosqualityQ1
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.relation.ispartofEuropean Journal of Pediatricsen_US
dc.relation.journalEuropean Journal of Pediatricsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAcute Renal Failureen_US
dc.subjectChildhooden_US
dc.subjectGlycogen Storage Disease Type Ven_US
dc.subjectRhabdomyolysisen_US
dc.subjectTreatmenten_US
dc.titleAcute Renal Failure due to Rhabdomyolysis in a Child with McArdle Diseaseen_US
dc.typeArticleen_US
dspace.entity.typePublication

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