Publication: Acute Renal Failure due to Rhabdomyolysis in a Child with McArdle Disease
| dc.authorscopusid | 36979398000 | |
| dc.authorscopusid | 10642354300 | |
| dc.authorscopusid | 56510123000 | |
| dc.authorscopusid | 6701319607 | |
| dc.authorscopusid | 6505879209 | |
| dc.authorscopusid | 59606045500 | |
| dc.contributor.author | Delibaş, A. | |
| dc.contributor.author | Bek, K. | |
| dc.contributor.author | Ezgü, F.S. | |
| dc.contributor.author | Demircin, G. | |
| dc.contributor.author | Oksal, A. | |
| dc.contributor.author | Öner, A. | |
| dc.date.accessioned | 2020-06-21T15:13:19Z | |
| dc.date.available | 2020-06-21T15:13:19Z | |
| dc.date.issued | 2008 | |
| dc.department | Ondokuz Mayıs Üniversitesi | en_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, Turkey | en_US |
| dc.description.abstract | Rhabdomyolysis 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.doi | 10.1007/s00431-007-0591-z | |
| dc.identifier.endpage | 940 | en_US |
| dc.identifier.issn | 0340-6199 | |
| dc.identifier.issn | 1432-1076 | |
| dc.identifier.issue | 8 | en_US |
| dc.identifier.pmid | 17899190 | |
| dc.identifier.scopus | 2-s2.0-46149088480 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.startpage | 939 | en_US |
| dc.identifier.uri | https://doi.org/10.1007/s00431-007-0591-z | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/19224 | |
| dc.identifier.volume | 167 | en_US |
| dc.identifier.wos | WOS:000257204200014 | |
| dc.identifier.wosquality | Q1 | |
| dc.language.iso | en | en_US |
| dc.publisher | Springer | en_US |
| dc.relation.ispartof | European Journal of Pediatrics | en_US |
| dc.relation.journal | European Journal of Pediatrics | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Acute Renal Failure | en_US |
| dc.subject | Childhood | en_US |
| dc.subject | Glycogen Storage Disease Type V | en_US |
| dc.subject | Rhabdomyolysis | en_US |
| dc.subject | Treatment | en_US |
| dc.title | Acute Renal Failure due to Rhabdomyolysis in a Child with McArdle Disease | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication |
