Shibuya, Makiko Iwamoto, Rie Kimura, Yukifumi Kamekura, Nobuhito Fujisawa, Toshiaki
Published in
Anesthesia progress
We report a case involving intravenous sedation for third molar extractions in a 32-year-old man with citrullinemia type I (CTLN1), a genetic disorder that affects the urea cycle. The patient was diagnosed with CTLN1 after he exhibited seizures soon after birth and was intellectually disabled because of persistent hyperammonemia, although his recen...
Posset, Roland Kölker, Stefan Gleich, Florian Okun, Jürgen G Gropman, Andrea L Nagamani, Sandesh C S Scharre, Svenja Probst, Joris Walter, Magdalena E Hoffmann, Georg F
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Published in
Molecular genetics and metabolism
The implementation of newborn screening (NBS) programs for citrullinemia type 1 (CTLN1) and argininosuccinic aciduria (ASA) is subject to controversial debate. The aim of this study was to assess the impact of NBS on the metabolic disease course and clinical outcome of affected individuals. In 115 individuals with CTLN1 and ASA, we compared the sev...
Shanmugam, Naresh P. Valamparampil, Joseph J. Reddy, Mettu Srinivas Al Said, Khoula Julenda Al-Thihli, Khalid Al-Hashmi, Nadia Al-Jishi, Emtithal Isa, Hasan Mohamed Ali Jalan, Anil B. Rela, Mohamed
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Published in
JIMD Reports
Purpose : Auxiliary partial orthotopic liver transplantation (APOLT) in metabolic liver disease (MLD) has the advantage of correcting the metabolic defect, preserving the native liver for gene therapy in the future with the possibility of withdrawal of immunosuppression. Methods : Retrospective analysis of safety and efficacy of APOLT in correcting...
Uebayashi(Yoshitoshi), Elena Yukie
京都大学 / 0048 / 新制・課程博士 / 博士(医学) / 甲第20661号 / 医博第4271号 / 新制||医||1024(附属図書館) / 京都大学大学院医学研究科医学専攻 / (主査)教授 川口 義弥, 教授 柳田 素子, 教授 斎藤 通紀 / 学位規則第4条第1項該当 / Doctor of Medical Science / Kyoto University / DFAM
Martín-Hernández, Elena Aldámiz-Echevarría, Luis Castejón-Ponce, Esperanza Pedrón-Giner, Consuelo Couce, María Luz Serrano-Nieto, Juliana Pintos-Morell, Guillem Bélanger-Quintana, Amaya Martínez-Pardo, Mercedes García-Silva, María Teresa
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Published in
Orphanet Journal of Rare Diseases
BackgroundAdvances in the diagnosis and treatment of urea cycle disorders (UCDs) have led to a higher survival rate. The purpose of this study is to describe the characteristics of patients with urea cycle disorders in Spain.MethodsObservational, cross-sectional and multicenter study. Clinical, biochemical and genetic data were collected from patie...
Wu, Tong-Fei Liu, Yu-Peng Li, Xi-Yuan Wang, Qiao Song, Jin-Qing Yang, Yan-Ling
Published in
Brain and Development
BackgroundArgininosuccinate synthetase deficiency (citrullinemia type 1) is a rare autosomal recessive disorder of the urea cycle characterized by elevated concentrations of citrulline, ammonia, and orotic acid, manifesting with acute hyperammonemic crises, usually early in life, with concurrent neurologic deterioration. Only a few cases of citrull...