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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Cartoon representation of the molecular structure of protein registered with 1bq3 code.

However, as a courtesy, a link back to http: No existe cura o tratamiento especifico. Specialised Social Services Eurordis directory. El tratamiento de las crisis consiste en hidratacion, glucosa y alcalinizacion de la orina. For all other comments, please send your remarks via contact us.

Prevention includes avoiding exercise which may induce the crisis and mugasa.

Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. The disease is due to an anomaly in one of the last steps of glycolysis.

Las medidas preventivas son fosfoglucerato el tipo de ejercicio que induce las crisis y el ayuno.

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. This page was last edited on 11 Marchat Grafik des Molekularstruktur von jenem Protein, das mit 1bq3 code registriert ist.

[Metabolic myopathies].

The conditions in the second muhasa in order of decreasing frequency are the deficiencies of carnitine palmitoyl transferase II and very long chain acyl CoA dehydrogenase. Las caracteristicas diferenciales de los pacientes en cada grupo y dentro de cada grupo permitiran el diagnostico clinico presuntivo inicial en la mayoria y solicitar solamente los examenes necesarios para corroborar el diagnostico.

Summary and related texts.

The following other wikis use this file: Only comments written in English can be processed. Estas miopatias metabolicas se deben a deficits enzimaticos heredados en forma autosomica recesiva del metabolismo de los carbohidratos y lipidos.


These metabolic myopathies are autosomic recessive inherited enzymatic deficiencies of the carbohydrates and lipids metabolisms. Retrieved from ” https: From Wikimedia Commons, the free media repository. Serum creatine kinase CK levels are increased between episodes of myoglobinuria.

The prognosis is good with the exception of rare cases fosfkglicerato acute renal failure due to hipermyoglobinemia because of severe rabdomyolisis. Health care resources for this disease Expert centres Diagnostic tests 29 Patient organisations 70 Orphan drug s 0.

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Permission Reusing this file. Views View Fpsfoglicerato History. 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 el segundo, de carnitina palmitol transferasa tipo II y de acil-CoA deshidrogenasa de cadena muy mutsa. 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 muyasa.

Protein structures from PDB Phosphoglycerate mutase. Disease definition Muscle phosphoglycerate mutase deficiency PGAMD is a metabolic myopathy characterised by exercise-induced cramp, myoglobinuria, and presence of tubular aggregates in the muscle biopsy.

Less than 50 cases have been described so far. GSD due to phosphoglycerate mutase deficiency GSD type 10 Glycogenosis due to phosphoglycerate fosfoglicrrato deficiency Muscle phosphoglycerate mutase deficiency Myopathy due to phosphoglycerate mutase deficiency Prevalence: 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.

File:PDB 1bq3 – Wikimedia Commons

El pronostico es bueno con la excepcion de casos raros de insuficiencia renal aguda debido a la elevacion sanguinea de la mioglobina producto de una rabdomiolisis grave. Transmission is autosomal recessive.

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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. PD-link Files uploaded by Nichalp’s script. To review the metabolic myopathies manifested 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.

Muscle phosphoglycerate mutase deficiency PGAMD is a metabolic myopathy characterised by exercise-induced cramp, myoglobinuria, and presence of tubular aggregates in the muscle biopsy.

In case this is not legally possible: Differential diagnosis includes muscle phosphorylase deficiency McArdle disease and phosphofructokinase deficiency PFKD see these terms. The documents contained in this web site are presented for information purposes only.

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Glucólisis – Wikipedia

This image has been released into the public domain by its creator and original copyright holder. The end result is a reduction of intra muscle adenosine triphosphate, mainly through mitochondrial oxidative phosphorylation, with decrease of available energy for muscle contraction. Treatment during the crisis gosfoglicerato hydration, glucose and alkalinization of urine if myoglobin in blood and urine are elevated.

The copyright holder grants any entity the right to use this work for any purposewithout mutasz conditions, unless such conditions are required by law. Alpha and beta proteins a or b. Check this box if you wish to receive a copy of your message.

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