Living donor liver transplantation from a heterozygous parent for classical maple syrup urine disease

Pediatric Transplantation

Volumn 19, Issue 3, 2015, Pages E66-E69

  Kadohisa, Masashi ^a   Matsumoto, Shirou ^a   Sawada, Hirotake ^b   Honda, Masaki ^a   Murokawa, Takahiro ^a   Hayashida, Shintaro ^a   Ohya, Yuki ^a   Lee, Kwang Jong ^a   Yamamoto, Hidekazu ^a   Mitsubuchi, Hiroshi ^a   Endo, Fumio ^a   Inomata, Yukihiro ^a  

^a KUMAMOTO UNIVERSITY   (Japan)

^b UNIVERSITY OF MIYAZAKI   (Japan)

Author keywords

autosomal recessive; branched chain alpha keto acid dehydrogenase complex; branched chain amino acids; hereditary metabolic disorder; heterozygote

Indexed keywords

2 OXOISOVALERATE DEHYDROGENASE (LIPOAMIDE); ENEMA; ISOLEUCINE; LEUCINE; VALINE; BRANCHED CHAIN AMINO ACID;

ARTICLE; ARTIFICIAL MILK; BLOOD GAS ANALYSIS; BODY WEIGHT; BREECH PRESENTATION; CASE REPORT; CELL LYSATE; CESAREAN SECTION; COLD ISCHEMIA; CONTROLLED STUDY; DIET RESTRICTION; DISEASE SEVERITY; ENZYME ACTIVITY; ENZYME BLOOD LEVEL; FATTY LIVER; FEMALE; GESTATIONAL AGE; HEART MUSCLE ISCHEMIA; HETEROZYGOTE; HUMAN; HUMAN CELL; INFANT; INTESTINE OBSTRUCTION; INTESTINE RESECTION; LIVER BIOPSY; LIVER FUNCTION; LIVER TRANSPLANTATION; LIVING DONOR; LIVING DONOR LIVER TRANSPLANTATION; LYMPHOCYTE; MAPLE SYRUP URINE DISEASE; MASS SCREENING; METABOLIC ACIDOSIS; OPERATION DURATION; POSTOPERATIVE PERIOD; PREOPERATIVE PERIOD; PROTEIN INTAKE; TANDEM MASS SPECTROMETRY; VOMITING; WEIGHT GAIN; FATHER; GENETICS; MALE; METABOLISM; PROCEDURES; TREATMENT OUTCOME;

AMINO ACIDS, BRANCHED-CHAIN; FATHERS; FEMALE; HETEROZYGOTE; HUMANS; INFANT; LIVER TRANSPLANTATION; LIVING DONORS; MALE; MAPLE SYRUP URINE DISEASE; POSTOPERATIVE PERIOD; TREATMENT OUTCOME;

EID: 84925871332     PISSN: 13973142     EISSN: 13993046     Source Type: Journal    
DOI: 10.1111/petr.12447     Document Type: Article

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