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Long-term outcomes in a 25-year-old female affected with lipin-1 deficiency.
Stepien, Karolina M; Schmidt, Wolfgang M; Bittner, Reginald E; O'Toole, Orna; McNamara, Brian; Treacy, Eileen P.
Afiliación
  • Stepien KM; Mark Holland Metabolic Unit, Adult Inherited Metabolic Diseases Salford Royal NHS Foundation Trust Salford United Kingdom.
  • Schmidt WM; Neuromuscular Research Department Center for Anatomy and Cell Biology, Medical University of Vienna Vienna Austria.
  • Bittner RE; Neuromuscular Research Department Center for Anatomy and Cell Biology, Medical University of Vienna Vienna Austria.
  • O'Toole O; Department of Neurology Mercy University Hospital Cork Ireland.
  • McNamara B; Department of Clinical Neurophysiology Cork University Hospital Cork Ireland.
  • Treacy EP; University College Dublin Dublin Ireland.
JIMD Rep ; 46(1): 4-10, 2019 Mar.
Article en En | MEDLINE | ID: mdl-31240148
Lipin-1 is a phosphatidic acid phosphohydrolase (EC 3.1.3.4) that catalyzes the dephosphorylation of phosphatidic acid to diacylglycerol and inorganic phosphate. Deficiency of this enzyme causes potentially fatal severe, recurrent episodes of rhabdomyolysis triggered by infection. The defect has only recently been recognized so little is known about the long-term outcome in adult patients with this disorder. We report the course and outcome of a 25-year-old female patient with lipin-1 deficiency after a recent episode of rhabdomyolysis requiring intensive care admission with a peak creatine kinase of 500 000 IU/L. One-year post discharge from intensive care, the patient has residual drop foot bilaterally consistent with bilateral common peroneal neuropathies in addition to a background residual distal myopathy.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: JIMD Rep Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: JIMD Rep Año: 2019 Tipo del documento: Article
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