Lipin-1 Deficiency-Associated Recurrent Rhabdomyolysis and Exercise-Induced Myalgia Persisting into Adulthood: A Case Report and Review of Literature

Phosphatidate phosphatase-1 (lipin-1) is encoded by LPIN1 gene. Lipin-1 deficiency has been reported as the second most common cause of early-onset rhabdomyolysis after primary fatty acid oxidation disorders. We report a case of a 32-year-old Sri Lankan female with a history of more than 10 episodes...

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Detalles Bibliográficos
Autores principales: Indika, Neluwa Liyanage Ruwan, Vidanapathirana, Dinesha Maduri, Jasinge, Eresha, Waduge, Roshitha, Shyamali, Narangoda Liyanage Ajantha, Perera, Poruthotage Pradeep Rasika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275236/
https://www.ncbi.nlm.nih.gov/pubmed/32549891
http://dx.doi.org/10.1155/2020/7904190

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275236/
https://www.ncbi.nlm.nih.gov/pubmed/32549891
http://dx.doi.org/10.1155/2020/7904190

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