FOSFOGLICERATO MUTASA PDF
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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fosfoglicerato-mutasa – English translation – Spanish-English dictionary
The disease is due to an cosfoglicerato in one of the last steps of glycolysis. Specialised Social Services Eurordis directory. Protein structures from PDB Phosphoglycerate mutase.
The prognosis is good with the exception of rare cases of acute muttasa failure due to hipermyoglobinemia because of severe rabdomyolisis. Serum creatine kinase CK levels are increased between episodes of myoglobinuria. 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: 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 fosfogllicerato final diagnosis.
From Wikimedia Commons, the free media repository. These metabolic myopathies are autosomic recessive inherited enzymatic deficiencies of the carbohydrates and lipids metabolisms. 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. In case this is not legally possible: Estas miopatias metabolicas se deben a deficits enzimaticos heredados en forma autosomica recesiva del metabolismo de los carbohidratos y lipidos.
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.
El tratamiento de las crisis consiste en hidratacion, glucosa y alcalinizacion de la orina.
This image has fosfoylicerato released into the public domain by its creator and original copyright holder. Retrieved from ” https: Las medidas preventivas son evitar el tipo de ejercicio que induce las crisis y el ayuno. Cartoon representation of the molecular structure of protein registered with 1bq3 code. Permission Reusing this file.
The conditions in the second group fosflglicerato order of decreasing frequency are the deficiencies of carnitine palmitoyl transferase II and very long chain acyl CoA dehydrogenase. Check this box if you wish to receive a copy of your message. However, as a courtesy, a link back to http: Views View Edit History. 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.
Transmission is autosomal recessive.
Treatment during the crisis includes hydration, glucose and alkalinization of urine if myoglobin in blood and urine are elevated.
Other search option s Alphabetical list. Differential diagnosis includes muscle phosphorylase deficiency McArdle disease and phosphofructokinase deficiency PFKD see these terms. The end result is a reduction of intra muscle adenosine triphosphate, mainly through mitochondrial oxidative phosphorylation, with decrease of available energy for muscle contraction.
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