Cargando…
PFKM gene defect and glycogen storage disease GSDVII with misleading enzyme histochemistry
OBJECTIVE: To elaborate the diagnostic methods used as “gold standard” in one of the most common glycogen storage diseases (GSDs), Tarui disease (GSDVII). METHODS: Two siblings with disease suggestive of GSD underwent thorough clinical analysis, including muscle biopsy, muscle MRI, exercise tests, l...
Autores principales: | Auranen, Mari, Palmio, Johanna, Ylikallio, Emil, Huovinen, Sanna, Paetau, Anders, Sandell, Satu, Haapasalo, Hannu, Viitaniemi, Kati, Piirilä, Päivi, Tyynismaa, Henna, Udd, Bjarne |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821086/ https://www.ncbi.nlm.nih.gov/pubmed/27066546 http://dx.doi.org/10.1212/NXG.0000000000000007 |
Ejemplares similares
-
Unique Exercise Lactate Profile in Muscle Phosphofructokinase Deficiency (Tarui Disease); Difference Compared with McArdle Disease
por: Piirilä, Päivi, et al.
Publicado: (2016) -
Recessive PYROXD1 mutations cause adult-onset limb-girdle-type muscular dystrophy
por: Sainio, Markus T., et al.
Publicado: (2018) -
Diagnostically important muscle pathology in DNAJB6 mutated LGMD1D
por: Sandell, Satu, et al.
Publicado: (2016) -
Absence of NEFL in patient-specific neurons in early-onset Charcot-Marie-Tooth neuropathy
por: Sainio, Markus T., et al.
Publicado: (2018) -
CHCHD10 variant p.(Gly66Val) causes axonal Charcot-Marie-Tooth disease
por: Auranen, Mari, et al.
Publicado: (2015)