Literature DB >> 26195537

An Adolescent Case of Citrin Deficiency With Severe Anorexia Mimicking Anorexia Nervosa.

Satsuki Takeuchi1, Masahide Yazaki2, Shinji Yamada1, Tetsuhiro Fukuyama3, Akio Inui4, Yasushi Iwasaki1, Shu-ichi Ikeda5.   

Abstract

We report a 12-year-old female citrin-deficient patient presenting with severe anorexia and body weight loss, mimicking the restricting type of anorexia nervosa (AN). She showed normal development until age 10 years when she started to play volleyball at school. She then became gradually anorexic, and her growth was stunted. At age 12, she was admitted to hospital because of severe anorexia and thinness. She was first thought to have AN, and drip infusion of glucose solution and high-calorie drinks were given, but her condition deteriorated further. She had a history of neonatal hepatitis and was therefore suspected to have citrin deficiency (CD). Genetic analysis of SLC25A13 revealed that she was compound heterozygous for 851del4 and IVS16ins3kb, and a diagnosis of CD was made. A low-carbohydrate diet with oral intake of arginine and ursodeoxycholic acid was started, and her condition gradually improved. The clinical features in our patient were similar to those of AN, and therefore AN may also be an important clinical sign in adolescent patients with CD.
Copyright © 2015 by the American Academy of Pediatrics.

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Year:  2015        PMID: 26195537     DOI: 10.1542/peds.2014-4172

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  5 in total

1.  A next generation sequencing gene panel for use in the diagnosis of anorexia nervosa.

Authors:  Maria Rachele Ceccarini; Vincenza Precone; Elena Manara; Stefano Paolacci; Paolo Enrico Maltese; Valentina Benfatti; Kristjana Dhuli; Kevin Donato; Giulia Guerri; Giuseppe Marceddu; Pietro Chiurazzi; Laura Dalla Ragione; Tommaso Beccari; Matteo Bertelli
Journal:  Eat Weight Disord       Date:  2021-11-25       Impact factor: 4.652

2.  Blood glucose and insulin and correlation of SLC25A13 mutations with biochemical changes in NICCD patients.

Authors:  Chun-Ting Lu; Qi-Ping Shi; Ze-Jian Li; Jiong Li; Lie Feng
Journal:  Exp Biol Med (Maywood)       Date:  2017-05-18

3.  Molecular diagnosis of pediatric patients with citrin deficiency in China: SLC25A13 mutation spectrum and the geographic distribution.

Authors:  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
Journal:  Sci Rep       Date:  2016-07-11       Impact factor: 4.379

Review 4.  Genetic contributions to the etiology of anorexia nervosa: New perspectives in molecular diagnosis and treatment.

Authors:  Stefano Paolacci; Aysha Karim Kiani; Elena Manara; Tommaso Beccari; Maria Rachele Ceccarini; Liborio Stuppia; Pietro Chiurazzi; Laura Dalla Ragione; Matteo Bertelli
Journal:  Mol Genet Genomic Med       Date:  2020-05-05       Impact factor: 2.183

5.  Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders.

Authors:  Yasmin Bylstra; Jyn Ling Kuan; Weng Khong Lim; Jaydutt Digambar Bhalshankar; Jing Xian Teo; Sonia Davila; Bin Tean Teh; Steve Rozen; Ene-Choo Tan; Wendy Kein Meng Liew; Khung Keong Yeo; Patrick Tan; Seang Mei Saw; Ching-Yu Cheng; Stuart Cook; Roger Foo; Saumya Shekhar Jamuar
Journal:  Genet Med       Date:  2018-07-02       Impact factor: 8.822

  5 in total

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