نتایج جستجو برای: citrullinemia

تعداد نتایج: 234  

2016
Wei-Xia Lin Han-Shi Zeng Zhan-Hui Zhang Man Mao Qi-Qi Zheng Shu-Tao Zhao Ying Cheng Feng-Ping Chen Wang-Rong Wen Yuan-Zong Song

Citrin deficiency (CD) is a Mendelian disease due to biallelic mutations of SLC25A13 gene. Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) is the major pediatric CD phenotype, and its definite diagnosis relies on SLC25A13 genetic analysis. China is a vast country with a huge population, but the SLC25A13 genotypic features of CD patients in our country remains far from bein...

Journal: :Genetics and molecular research : GMR 2010
R Marquis-Nicholson E Glamuzina D Prosser C Wilson D R Love

We developed a mutation-screening protocol for the ASS1 gene in order to guide clinical management of neonates with elevated citrulline detected during routine newborn screening. An exon-based amplification and sequencing method was designed and successfully applied to patients to identify disease-associated mutations. The sequencing-based method was applied to three patients with mild or asymp...

Journal: :American journal of medical genetics. Part A 2008
David P Dimmock Pamela Trapane Annette Feigenbaum Catherine E Keegan Stephen Cederbaum James Gibson Michael J Gambello Keith Vaux Patricia Ward Gregory M Rice Jon A Wolff William E O'Brien Ping Fang

Expanded newborn screening detects patients with modest elevations in citrulline; however it is currently unclear how to treat these patients and how to counsel their parents. In order to begin to address these issues, we compared the clinical, biochemical, and molecular features of 10 patients with mildly elevated citrulline levels. Three patients presented with clinical illness whereas seven ...

2012
Suporn Treepongkaruna Suttiruk Jitraruch Porawee Kodcharin Dussadee Charoenpipop Pim Suwannarat Paneeya Pienvichit Keiko Kobayashi Duangrurdee Wattanasirichaigoon

BACKGROUND The most common causes of cholestatic jaundice are biliary atresia and idiopathic neonatal hepatitis (INH). Specific disorders underlying INH, such as various infectious and metabolic causes, including neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) especially, in East Asian populations are increasingly being identified. Since most NICCD infants recovered from l...

Journal: :The Journal of clinical investigation 1982
T S Su H G Bock A L Beaudet W E O'Brien

We have analyzed cultured skin fibroblasts derived from patients with argininosuccinate synthetase deficiency for alterations in gene structure, mRNA content, and protein structure. Genomic DNA was digested with the endonucleases EcoRI or HindIII, and the fragments were analyzed by Southern blotting and hybridization with a cDNA probe for argininosuccinate synthetase. The blot pattern is comple...

Journal: :The Southeast Asian journal of tropical medicine and public health 2003
Hye-Ran Yoon Kyung Ryul Lee Hohyun Kim Seungwoo Kang Yunmi Ha Dong Hwan Lee

Seoul Clinical Laboratories began screening newborns and high risk group blood spots with tandem mass spectrometry (MS/MS) in April 2001. The goal was to determine approximate prevalence of metabolic disorders and optimization of decision criteria for estimation of preventive effect with early diagnosis. Approximately 44,300 neonates and children were screened and the estimated prevalence (newb...

2014
Shane C. Quinonez Andrea H. Seeley Mary Seeterlin Eleanor Stanley Ayesha Ahmad

Dihydrolipoamide dehydrogenase deficiency, also known as maple syrup urine disease (MSUD) type III, is caused by the deficiency of the E3 subunit of branched chain alpha-ketoacid dehydrogenase (BCKDH), α-ketoglutarate dehydrogenase (αKGDH), and pyruvate dehydrogenase (PDH). DLD deficiency variably presents with either a severe neonatal encephalopathic phenotype or a primarily hepatic phenotype....

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