Cargando…
Recurrent Rhabdomyolysis, Acute Kidney Injury, and Foot Drop: A Rare Case with Mitochondrial Trifunctional Protein (MTP) Deficiency
Autores principales: | Dabla, Surekha, Wangnoo, Areca, Kumar, Neeraj, Bala, Kiran |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996484/ https://www.ncbi.nlm.nih.gov/pubmed/36911475 http://dx.doi.org/10.4103/aian.aian_606_22 |
Ejemplares similares
-
Novel mutations in the
HADHB
gene causing a mild phenotype of mitochondrial trifunctional protein (MTP) deficiency
por: Ørstavik, Kristin, et al.
Publicado: (2022) -
Fatal pitfalls in newborn screening for mitochondrial trifunctional protein (MTP)/long-chain 3-Hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency
por: Lotz-Havla, Amelie S., et al.
Publicado: (2018) -
Reversible sensory neuropathy in mitochondrial trifunctional protein deficiency
por: Grünert, Sarah Catharina, et al.
Publicado: (2022) -
Using Mitochondrial Trifunctional Protein Deficiency to Understand Maternal Health
por: Miklas, Jason W., et al.
Publicado: (2020) -
Efficacy of bezafibrate in two patients with mitochondrial trifunctional protein deficiency
por: Suyama, Tomonori, et al.
Publicado: (2020)