The severe infantile form may lead to sudden death during infancy due, in general, to paroxysmal cardiac arrhythmias. File:Carnitine — Wikimedia Commons You can change the settings or obtain more information by clicking here. Other search option s Alphabetical list. The treatment is to avoid the factors that can trigger rhabdomyolysis, like prolonged fasting, to eating a low-fat high-carbohydrate diet, frequent meals and with excessive carbohydrates intake after exercise. Metabolic causes of mioglobinuria. The clinical picture consists of recurrent episodes of muscular weakness, myalgias, rhabdomyolysis or acute renal failure.
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Deficiencia de carnitina palmitoiltransferasa tipo II — Wikipedia, la enciclopedia libre Forty-eight hours later he developed progressive increase of creatinine values to 5. Detailed information Professionals Clinical genetics review English The clinical picture consists of recurrent episodes of muscular weakness, myalgias, rhabdomyolysis or acute renal failure. Metabolic causes of mioglobinuria. Physical examination was unremarkable except for hyperemic pharynx and intense pain on muscle palpation.
SerLeu mutation, which impairs enzyme stability. Health care resources for this disease Expert centres Diagnostic tests Patient organisations 67 Orphan drug s 1. The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years. If the disease-causing mutations are identified in an affected individual, early diagnosis by molecular genetic testing can be offered to at-risk relatives to reduce morbidity and mortality.
The treatment is to avoid the factors that can trigger rhabdomyolysis, like prolonged fasting, to eating a low-fat high-carbohydrate diet, frequent meals and with excessive carbohydrates intake after exercise. This work is licensed under a Creative Commons Attribution 4.
Only comments written in English can be processed. Differential diagnosis The differential diagnosis should include McArdle disease, Duchenne muscular dystrophy, cytochrome c oxidase deficiency see these termscomplex II deficiency, complex III deficiency and rhabdomyolysis due to excessive exercise, infections, autoimmune reactions or drug-related neuroleptic syndrome among others. Clinical description The myopathic form is the least severe and is characterized by recurrent attacks of rhabdomyolysis, muscle pain and weakness triggered by prolonged physical exercise, fasting, viral illness or extremes in temperature.
This condition is the most frequent cause of recurrent myoglobinuria with no clear trigger and should be always suspected in these patients. The disease is more common in men, probably reflecting an ascertainment bias related to exposure to prolonged exercise. Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. Deficiencia de carnitina palmitoiltransferasa tipo II Manitol use in acute renal failure is controversial, but in case of rhabdomyolysis it appears to reduce interstitial edema and lalmitoil uptake free radicals.
Profilaxis del fracaso renal agudo. The severe infantile form is characterized by a severe fasting intolerance leading to metabolic disorders such as hypoketotic hypoglycemia and hepatic encephalopathy. The consequence is muscle destruction or rhabdomyolysis. Transferada are asymptomatic between episodes of rhabdomyolysis.
Myoglobinuria and carnitine palmitoil tranferase deficiency in father and son. File:Carnitine structure. In the 9th day the patient recovered diuresis. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.
The differential diagnosis should include McArdle disease, Duchenne muscular dystrophy, cytochrome c oxidase deficiency see these termscomplex II deficiency, complex III deficiency and rhabdomyolysis due to excessive exercise, infections, autoimmune reactions or drug-related carnitiha syndrome among cwrnitina.
The journal accepts submissions of articles in English and in Spanish languages. Carnitine palmitoil tranferase transferrasa in pregnancy, a case report. CiteScore measures average citations received per document published. 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.
SRJ is a prestige metric based on the idea that not all citations are the same. Si continua navegando, consideramos que acepta su uso. L-carnitine administration and anaplerotic diet therapy with triheptanoin have been suggested for treatment of the disease; however benefits have not been proven.
He was evaluated at the Emergency Room because of generalized muscle pain and odynophagia. The documents contained trasferasa this web site are presented for information purposes only. Carnitine palmitoiltransferase deficiency in a collage transferasz Previous article Next article. Additional information Further information on this disease Classification s ccarnitina Gene s 1 Clinical signs and symptoms Publications in PubMed Other website s 9.
However they are a preventable cause of acute renal failure, which very often goes unnoticed. J Am Coll Health Transmission is autosomal recessive. More than CPT II cases have been described with the myopathic form being the most common myopathic form: Rhabdomyolysis and myoglobinuric acute renal failure. Summary and related texts. For all other comments, please send your remarks via contact us.
The Journal publishes articles on basic or clinical research relating to nephrology, arterial hypertension, dialysis and kidney transplants. Most Related.
Deficiencia de carnitina palmitoiltransferasa tipo II
Deficiencia de carnitina palmitoiltransferasa II