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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Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. The documents contained in this web site are presented for information purposes only. The following other wikis use this file: By fosfoglicsrato this site, you agree to the Terms of Use and Privacy Policy.

Health care resources for this disease Expert centres Diagnostic tests 29 Patient organisations 70 Orphan drug s 0. This page was last edited on 11 Marchat Los deficits enzimaticos en el primer grupo son de miofosforilasa glucogenosis Vfosfofructocinasa muscular glucogenosis VIIfosfoglicerato mutasa 1 glucogenosis X y beta enolasa glucogenosis XIIIy en fosflglicerato segundo, de carnitina palmitol transferasa tipo Muasa y de acil-CoA deshidrogenasa de cadena muy larga.

El resultado final es una reduccion del trifosfato de adenosina principalmente a traves de la fosforilacion oxidativa mitocondrial con disminucion de la energia disponible para la contraccion muscular.

Term Bank – fosfoglicerato-mutasa – Spanish English Dictionary

Differential diagnosis includes muscle phosphorylase deficiency McArdle disease and phosphofructokinase deficiency PFKD see these terms. 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 dosfoglicerato necessary tests to achieve the final diagnosis. The material is in no way intended to replace professional medical fosfogglicerato by a qualified specialist and should not be used as a basis for diagnosis or treatment.


El tratamiento de las crisis consiste en hidratacion, glucosa y alcalinizacion de la orina. Retrieved from ” https: 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.

“fosfoglicerato-mutasa” in English

From Wikimedia Commons, the free media repository. GSD due to phosphoglycerate mutase deficiency GSD type 10 Glycogenosis due to phosphoglycerate fosfogliferato deficiency Muscle phosphoglycerate mutase deficiency Myopathy due to phosphoglycerate mutase deficiency Prevalence: The disease is due to an anomaly in one of the last steps of glycolysis.

Disease definition Muscle phosphoglycerate mutase mutxsa PGAMD is a metabolic myopathy characterised by exercise-induced cramp, myoglobinuria, and presence of tubular aggregates in the muscle biopsy. Serum creatine kinase CK levels are increased between episodes of myoglobinuria.


Views View Edit History. Prevention includes avoiding exercise which may induce the crisis and fasting. The conditions in the second group in order of decreasing frequency are the deficiencies of carnitine palmitoyl transferase II and very long fosfoglicerxto acyl CoA dehydrogenase.


The end result is a reduction of intra muscle adenosine triphosphate, mainly through mitochondrial oxidative phosphorylation, with decrease of available energy for muscle contraction. No existe cura o tratamiento especifico. Treatment during the crisis includes hydration, glucose and alkalinization of urine if myoglobin in blood and urine are elevated.

Cartoon representation of the molecular structure of protein registered with 1bq3 code. Less than 50 cases have been described so far. This image has been released into the public domain by its creator and original copyright holder.

Alpha and beta proteins a or b. Check this box if you wish to receive a copy of your message.

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Only comments written in English can be processed. For all other comments, please send your remarks via contact us. The prognosis is good with the exception of rare cases of acute 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. Estas miopatias metabolicas se deben a deficits enzimaticos heredados en forma autosomica recesiva del metabolismo de los carbohidratos y lipidos.