Translation for ‘fosfoglicerato-mutasa’ in the free Spanish-English dictionary and many other English translations. Montse Mendoza. Updated 4 December Transcript. Ciclo de Krebs. Citratosintetasa. Oxalacetato. Gluconeogénesis. Ciclo de Cori. Balam Vargas Peñaloza. Updated 18 September Transcript. Fosfoglicerato mutasa. Fosfoglucomutasa.
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The differential characteristics of patients in each group and within each group will allow to make the initial presumptive clinical diagnosis in the majority and then to order only the necessary tests to achieve the final diagnosis. Alpha and beta proteins a or b.
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The disease is due to an anomaly in one of the last steps of glycolysis.
Term Bank – fosfoglicerato-mutasa – Spanish English Dictionary
Estas miopatias metabolicas se deben a deficits enzimaticos heredados en forma autosomica recesiva del metabolismo de los carbohidratos y lipidos.
El tratamiento de las crisis consiste en hidratacion, glucosa y alcalinizacion de la orina. No existe cura o tratamiento especifico. The following other wikis use this file: Muscle phosphoglycerate mutase deficiency PGAMD is a metabolic myopathy characterised by exercise-induced cramp, myoglobinuria, and presence of tubular aggregates in the muscle biopsy.
The prognosis is good with the exception of rare cases of foscoglicerato renal failure due to hipermyoglobinemia because of severe rabdomyolisis. Las medidas preventivas son evitar el tipo de ejercicio que induce las crisis y el ayuno. Permission Reusing this file.
This image has been released into the public domain by its creator and original copyright holder. Transmission is autosomal recessive. However, as a courtesy, a link back to http: The conditions in the second group in order of decreasing frequency are the deficiencies of carnitine palmitoyl transferase II and very long chain acyl CoA dehydrogenase.
These metabolic myopathies are autosomic recessive inherited enzymatic deficiencies of the carbohydrates and lipids metabolisms. Retrieved from ” https: The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
Treatment during the crisis includes hydration, glucose and alkalinization of urine if myoglobin in blood and urine are elevated. As such you are entirely free to reproduce it, create derivative works, or make commercial use of it as you see fit, without any requirement to give the creator credit.
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Summary and related texts. Prevention includes avoiding exercise which may induce the crisis and fasting.
To review the metabolic myopathies fosoglicerato only by crisis of myalgias, cramps and rigidity of the muscles with decreased voluntary contractions and normal inter crisis neurologic examination in children and adolescents.
Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. The end result is a reduction of intra muscle adenosine triphosphate, mainly through mitochondrial oxidative phosphorylation, with decrease of available energy for muscle contraction.
From Wikimedia Commons, the free media repository. GSD due to phosphoglycerate mutase deficiency GSD type 10 Glycogenosis due to phosphoglycerate mutase deficiency Muscle phosphoglycerate mutase deficiency Myopathy due to phosphoglycerate mutase deficiency Prevalence: This page was last edited on 11 Marchat