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

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.

For all other comments, please send your remarks via contact us. 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: 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.

Rutas metabólicas by Montse Mendoza on Prezi

The documents contained in this web site are presented for information purposes only. Check this box if you wish to receive a copy of your message. Differential diagnosis includes muscle phosphorylase deficiency McArdle disease and phosphofructokinase deficiency PFKD see these terms.

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 larga. Transmission is autosomal recessive.

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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. By using this site, you agree to the Terms of Use and Privacy Policy. The end result is a reduction of intra muscle adenosine triphosphate, mainly through mitochondrial oxidative phosphorylation, with decrease of available energy for muscle contraction.

File:PDB 1bq3 EBI.jpg

No existe cura o tratamiento especifico. 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. Summary and related texts. Specialised Social Services Eurordis directory. From Wikimedia Commons, the free media repository. Less than 50 cases have fosfoglicerayo described fosflglicerato far.

Other search option s Alphabetical list. Las medidas preventivas son evitar el tipo de ejercicio que induce las crisis y el ayuno. Prevention includes avoiding exercise which may induce the crisis and fasting. Serum creatine kinase CK levels are increased between episodes of myoglobinuria.

Rutas Metabolicas by Balam Vargas Peñaloza on Prezi

Cartoon representation of the molecular structure of protein registered with 1bq3 code. The following other wikis use this file: Protein structures from PDB Phosphoglycerate mutase.

Alpha and beta proteins a or b. Treatment during the crisis includes hydration, glucose and alkalinization of urine if myoglobin in blood and fosfogliceraato are elevated. Views View Edit History.

However, as a courtesy, a fozfoglicerato back to http: In case this is not legally possible: 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. Health care resources for this disease Expert centres Diagnostic tests 29 Patient organisations 70 Orphan drug s 0.

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These metabolic myopathies are autosomic recessive inherited enzymatic deficiencies of the carbohydrates and lipids metabolisms. Only comments seeking fodfoglicerato improve the quality and accuracy of information on the Orphanet website are accepted.

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. Grafik des Molekularstruktur von jenem Fosfoglicedato, das mit 1bq3 code registriert ist.

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.

Retrieved from ” https: This image mutsa been released into the public domain by its creator and original copyright holder. The copyright holder grants any entity the right to use this work for any purposewithout any conditions, unless such fosfoglicerago are required by law. This page was last edited on 11 Marchat