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Two tales of LPIN1 deficiency: from fatal rhabdomyolysis to favorable outcome of acute compartment syndrome.
Kahraman, Ayca Burcu; Karakaya, Bekir; Yildiz, Yilmaz; Kamaci, Saygin; Kesici, Selman; Simsek-Kiper, Pelin Ozlem; Kurt-Sukur, Eda Didem; Bayrakci, Benan; Haliloglu, Goknur.
Afiliación
  • Kahraman AB; Department of Pediatrics, Division of Metabolism and Nutrition, Hacettepe University Faculty of Medicine, Ankara TR06230, Turkey. Electronic address: aycakahraman@hacettepe.edu.tr.
  • Karakaya B; Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.
  • Yildiz Y; Department of Pediatrics, Division of Metabolism and Nutrition, Hacettepe University Faculty of Medicine, Ankara TR06230, Turkey.
  • Kamaci S; Department of Orthopedics and Travmatology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
  • Kesici S; Division of Intensive Care Unit, Hacettepe University Faculty of Medicine, Ankara, Turkey.
  • Simsek-Kiper PO; Division of Genetics, Hacettepe University Faculty of Medicine, Ankara, Turkey.
  • Kurt-Sukur ED; Division of Nephrology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
  • Bayrakci B; Division of Intensive Care Unit, Hacettepe University Faculty of Medicine, Ankara, Turkey.
  • Haliloglu G; Division of Neurology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Neuromuscul Disord ; 32(11-12): 931-934, 2022 12.
Article en En | MEDLINE | ID: mdl-36195520
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Rabdomiólisis / Síndromes Compartimentales Tipo de estudio: Prognostic_studies Límite: Child, preschool / Humans Idioma: En Revista: Neuromuscul Disord Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article
Texto completo
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Rabdomiólisis / Síndromes Compartimentales Tipo de estudio: Prognostic_studies Límite: Child, preschool / Humans Idioma: En Revista: Neuromuscul Disord Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article