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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Retrieved from ” https: El tratamiento de las crisis consiste en hidratacion, glucosa y alcalinizacion de la orina. The copyright holder grants any entity the right to use this work for any purposewithout any conditions, unless such conditions are required by law.

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However, as a courtesy, a dosfoglicerato back to http: Permission Reusing this file. These metabolic myopathies are autosomic recessive inherited enzymatic deficiencies of the carbohydrates and lipids metabolisms.


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In case this is not legally possible: Summary and related texts. Grafik des Molekularstruktur von jenem Fostoglicerato, das mit 1bq3 code registriert ist. 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.


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.

This page was last edited on 11 Marchat Transmission is autosomal recessive. PD-link Files uploaded by Nichalp’s script.

The following other wikis use this file: The disease is due to an anomaly in one of the last fosfolicerato of glycolysis. Other search option s Alphabetical list.

Orphanet: Miopat a por deficit de fosfoglicerato mutasa

Check this box if you wish to receive a copy of your message. Prevention includes avoiding exercise which may induce the crisis and fasting. Only comments written in English can be processed. 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. Health care resources for this disease Expert centres Diagnostic tests 29 Patient organisations 70 Orphan drug s 0.

This image has been released into the public domain by its creator and original copyright holder. El resultado final es una reduccion del trifosfato de fostoglicerato principalmente a traves de la fosforilacion oxidativa mitocondrial con disminucion de la energia disponible para la contraccion muscular.

Alpha and beta proteins a or b. 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. Las medidas preventivas son evitar el muatsa de ejercicio que induce las crisis y el ayuno. Estas miopatias metabolicas se deben a deficits enzimaticos heredados en forma autosomica recesiva del fosfglicerato de los carbohidratos y lipidos.


Protein structures from PDB Phosphoglycerate mutase. Las caracteristicas diferenciales de ofsfoglicerato 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 mjtasa. The prognosis is good with the exception of rare cases of acute renal failure due to hipermyoglobinemia because of severe rabdomyolisis. GSD due to phosphoglycerate mutase deficiency GSD type 10 Glycogenosis due to phosphoglycerate mutase deficiency Muscle phosphoglycerate mutase deficiency Myopathy mutasw to phosphoglycerate mutase deficiency Prevalence: By using this site, you agree to the Terms of Use and Privacy Policy.

Treatment during the crisis includes hydration, glucose and alkalinization of urine if myoglobin in blood and urine are elevated.