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=> 2010-03-03 ) [11] => stdClass Object ( [ID] => 883 [post_parent] => 70 [post_title] => Guide to Galactosemia and Primary Ovarian Insufficiency (POI) [post_name] => galactosemia-and-primary-ovarian-insufficiency-poi [date] => 2010-01-05 ) [12] => stdClass Object ( [ID] => 74 [post_parent] => 5 [post_title] => Fatty Acid Oxidation Disorders [post_name] => fatty-acid-oxidation-disorders [date] => 2010-03-02 ) [13] => stdClass Object ( [ID] => 1010 [post_parent] => 883 [post_title] => Just for Parents - Your Guide to Talking to Your Daughter About Galactosemia and POI [post_name] => parents-daughter-galactosemia-poi [date] => 2010-01-06 ) [14] => stdClass Object ( [ID] => 1012 [post_parent] => 883 [post_title] => For Women with Galactosemia and POI - Your Guide to Taking Action [post_name] => guide-for-women-galactosemia-poi [date] => 2010-01-06 ) [15] => stdClass Object ( [ID] => 1014 [post_parent] => 883 [post_title] => Other Resources for Families and Women with Galactosemia and POI 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[post_parent] => 426 [post_title] => Ornithine Transcarbamylase Deficiency (OTC) [post_name] => ornithine-transcarbamylase-deficiency-otc [date] => 2009-10-30 ) [29] => stdClass Object ( [ID] => 953 [post_parent] => 9 [post_title] => Psychologists' Resources [post_name] => psychologists-resources [date] => 2009-12-24 ) [30] => stdClass Object ( [ID] => 443 [post_parent] => 426 [post_title] => Carbamyl Phosphate Synthetase Deficiency (CPS) [post_name] => carbamyl-phosphate-synthetase-deficiency-cps [date] => 2009-10-30 ) [31] => stdClass Object ( [ID] => 445 [post_parent] => 426 [post_title] => Argininosuccinic Acid Synthetase Deficiency (Citullinemia) (AS) [post_name] => argininosuccinic-acid-synthetase-deficiency-citullinemia-as [date] => 2009-10-30 ) [32] => stdClass Object ( [ID] => 447 [post_parent] => 426 [post_title] => Argininosuccinic Acid Lyase Deficiency (ASA) [post_name] => argininosuccinic-acid-lyase-deficiency-asa [date] => 2009-10-30 ) [33] => stdClass Object ( [ID] => 812 [post_parent] => 9 [post_title] => Transition to Adult Care [post_name] => transition-to-adult-care [date] => 2009-12-08 ) [34] => stdClass Object ( [ID] => 449 [post_parent] => 426 [post_title] => Arginase Deficiency [post_name] => arginase-deficiency [date] => 2009-10-30 ) [35] => stdClass Object ( [ID] => 430 [post_parent] => 123 [post_title] => Fatty Acid Oxidation Disorders [post_name] => fatty-acid-oxidation-disorders [date] => 2009-12-08 ) [36] => stdClass Object ( [ID] => 451 [post_parent] => 430 [post_title] => Very Long Chain Acyl-CoA Dehydrogenase Deficiency (VLCADD) [post_name] => very-long-chain-acyl-coa-dehydrogenase-deficiency-vlcadd [date] => 2009-11-02 ) [37] => stdClass Object ( [ID] => 453 [post_parent] => 430 [post_title] => Long Chain Hydroxy Acyl-CoA Dehydrogenase Deficiency ( LCHADD) [post_name] => long-chain-hydroxy-acyl-coa-dehydrogenase-deficiency-lchadd [date] => 2009-11-02 ) [38] => stdClass Object ( [ID] => 455 [post_parent] => 430 [post_title] => 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For Professionals
For Families

Deficiencia de la Deshidrogenasa del Acil-CoA de Cadena Corta (SCADD)

Este protocolo es para el niño enfermo que ha sido previamente diagnosticados con la deficiencia de la deshidrogenasa del acetil CoA de cadena corta (SCADD). Un defecto intramitocondrial de la ß-oxidación de los ácidos grasos causa la SCADD. Puede causar hipoglicemia grave y puede ser fatal. A continuación le mostramos un diagrama de la ruta metabólica de la ß-oxidación de los ácidos grasos que muestra en que lugar de esta ruta se encuentra el bloqueo de la SCADD.

Haga clic aquí para ver el protocolo completo en formato PDF.

Descargo de responsabilidad
El cuidado de los pacientes con trastornos del metabolismo es complejo y es fundamental que un especialista en metabolismo ponerse en contacto lo más rápidamente posible. Este protocolo es solamente una guía y no debe utilizarse para el tratamiento definitivo, sin consultar metabólico. Por favor, lea nuestro Condiciones de uso.