Literature DB >> 25663424

Asparagine Synthetase Deficiency: New Inborn Errors of Metabolism.

Majid Alfadhel1, Muhammad Talal Alrifai, Daniel Trujillano, Hesham Alshaalan, Ali Al Othaim, Shatha Al Rasheed, Hussam Assiri, Abdulrhman A Alqahtani, Manal Alaamery, Arndt Rolfs, Wafaa Eyaid.   

Abstract

BACKGROUND: Asparagine synthetase deficiency (ASD) is a newly identified neurometabolic disorder characterized by severe congenital microcephaly, severe global developmental delay, intractable seizure disorder, and spastic quadriplegia. Brain MRI showed brain atrophy, delayed myelination, and simplified gyriform pattern.
METHODS: We report ASD deficiency in a 2- and 4-year-old sibling. On them, we described clinical, biochemical, and molecular findings, and we compared our results with previously reported cases.
RESULTS: We identified a homozygous novel missense mutation in ASNS gene in both probands and we demonstrated low CSF and plasma asparagine in both patients.
CONCLUSIONS: Clinicians should suspect ASD deficiency in any newborn presented with severe congenital microcephaly followed by severe epileptic encephalopathy and global developmental delay. CSF asparagine level is low in this disorder while plasma may be low.

Entities:  

Year:  2015        PMID: 25663424      PMCID: PMC4486270          DOI: 10.1007/8904_2014_405

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  8 in total

1.  Cloning of cDNA for asparagine synthetase from rat Sertoli cell.

Authors:  S Hongo; T Chiyo; M Takeda
Journal:  Biochem Mol Biol Int       Date:  1996-02

2.  Molecular structure of the human asparagine synthetase gene.

Authors:  Y P Zhang; M A Lambert; A E Cairney; D Wills; P N Ray; I L Andrulis
Journal:  Genomics       Date:  1989-04       Impact factor: 5.736

3.  Congenital glutamine deficiency with glutamine synthetase mutations.

Authors:  Johannes Häberle; Boris Görg; Frank Rutsch; Eva Schmidt; Annick Toutain; Jean-François Benoist; Antoinette Gelot; Annie-Laure Suc; Wolfgang Höhne; Freimut Schliess; Dieter Häussinger; Hans G Koch
Journal:  N Engl J Med       Date:  2005-11-03       Impact factor: 91.245

4.  Creatine deficiency in the brain: a new, treatable inborn error of metabolism.

Authors:  S Stöckler; U Holzbach; F Hanefeld; I Marquardt; G Helms; M Requart; W Hänicke; J Frahm
Journal:  Pediatr Res       Date:  1994-09       Impact factor: 3.756

5.  Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiency.

Authors:  T Bourgeron; D Chretien; J Poggi-Bach; S Doonan; D Rabier; P Letouzé; A Munnich; A Rötig; P Landrieu; P Rustin
Journal:  J Clin Invest       Date:  1994-06       Impact factor: 14.808

6.  An update on serine deficiency disorders.

Authors:  S N van der Crabben; N M Verhoeven-Duif; E H Brilstra; L Van Maldergem; T Coskun; E Rubio-Gozalbo; R Berger; T J de Koning
Journal:  J Inherit Metab Dis       Date:  2013-03-06       Impact factor: 4.982

7.  Deficiency of asparagine synthetase causes congenital microcephaly and a progressive form of encephalopathy.

Authors:  Elizabeth K Ruzzo; José-Mario Capo-Chichi; Bruria Ben-Zeev; David Chitayat; Hanqian Mao; Andrea L Pappas; Yuki Hitomi; Yi-Fan Lu; Xiaodi Yao; Fadi F Hamdan; Kimberly Pelak; Haike Reznik-Wolf; Ifat Bar-Joseph; Danit Oz-Levi; Dorit Lev; Tally Lerman-Sagie; Esther Leshinsky-Silver; Yair Anikster; Edna Ben-Asher; Tsviya Olender; Laurence Colleaux; Jean-Claude Décarie; Susan Blaser; Brenda Banwell; Rasesh B Joshi; Xiao-Ping He; Lysanne Patry; Rachel J Silver; Sylvia Dobrzeniecka; Mohammad S Islam; Abul Hasnat; Mark E Samuels; Dipendra K Aryal; Ramona M Rodriguiz; Yong-Hui Jiang; William C Wetsel; James O McNamara; Guy A Rouleau; Debra L Silver; Doron Lancet; Elon Pras; Grant A Mitchell; Jacques L Michaud; David B Goldstein
Journal:  Neuron       Date:  2013-10-16       Impact factor: 17.173

8.  Asparagine synthetase deficiency detected by whole exome sequencing causes congenital microcephaly, epileptic encephalopathy and psychomotor delay.

Authors:  Salma Ben-Salem; Joseph G Gleeson; Aisha M Al-Shamsi; Barira Islam; Jozef Hertecant; Bassam R Ali; Lihadh Al-Gazali
Journal:  Metab Brain Dis       Date:  2014-09-17       Impact factor: 3.584

  8 in total
  20 in total

Review 1.  Antenatal manifestations of inborn errors of metabolism: biological diagnosis.

Authors:  Christine Vianey-Saban; Cécile Acquaviva; David Cheillan; Sophie Collardeau-Frachon; Laurent Guibaud; Cécile Pagan; Magali Pettazzoni; Monique Piraud; Antonin Lamazière; Roseline Froissart
Journal:  J Inherit Metab Dis       Date:  2016-07-08       Impact factor: 4.982

Review 2.  Asparagine synthetase: Function, structure, and role in disease.

Authors:  Carrie L Lomelino; Jacob T Andring; Robert McKenna; Michael S Kilberg
Journal:  J Biol Chem       Date:  2017-10-30       Impact factor: 5.157

Review 3.  Asparagine Synthetase deficiency-report of a novel mutation and review of literature.

Authors:  Neerja Gupta; Vishal Vishnu Tewari; Manoj Kumar; Nitika Langeh; Aditi Gupta; Pallavi Mishra; Punit Kaur; Vedam Ramprasad; Sakthivel Murugan; Reema Kumar; Manisha Jana; Madhulika Kabra
Journal:  Metab Brain Dis       Date:  2017-08-03       Impact factor: 3.584

Review 4.  Antenatal manifestations of inborn errors of metabolism: prenatal imaging findings.

Authors:  Laurent Guibaud; Sophie Collardeau-Frachon; Audrey Lacalm; Mona Massoud; Massimiliano Rossi; Marie Pierre Cordier; Christine Vianey-Saban
Journal:  J Inherit Metab Dis       Date:  2016-11-16       Impact factor: 4.982

5.  Characterization of a novel variant in siblings with Asparagine Synthetase Deficiency.

Authors:  Stephanie J Sacharow; Elizabeth E Dudenhausen; Carrie L Lomelino; Lance Rodan; Christelle Moufawad El Achkar; Heather E Olson; Casie A Genetti; Pankaj B Agrawal; Robert McKenna; Michael S Kilberg
Journal:  Mol Genet Metab       Date:  2017-12-20       Impact factor: 4.797

6.  Whole Exome Sequencing in a Rare Disease: A Patient with Anomalous Left Coronary Artery from the Pulmonary Artery (Bland-White-Garland Syndrome).

Authors:  Nezih Hekim; Talantbek Batyraliev; Daniel Trujillano; Wei Wang; Collet Dandara; Zarema Karben; Eyüp İlker Saygılı; Zafer Çetin; Deniz Mıhcıoğlu; Serdar Türkmen; Mehmet Ali İkidağ; Mehmet Ali Cüce; Arndt Rolfs
Journal:  OMICS       Date:  2016-05

7.  Elucidation of the complex metabolic profile of cerebrospinal fluid using an untargeted biochemical profiling assay.

Authors:  Adam D Kennedy; Kirk L Pappan; Taraka R Donti; Anne M Evans; Jacob E Wulff; Luke A D Miller; V Reid Sutton; Qin Sun; Marcus J Miller; Sarah H Elsea
Journal:  Mol Genet Metab       Date:  2017-04-09       Impact factor: 4.797

8.  Diaphragmatic Eventration in Sisters with Asparagine Synthetase Deficiency: A Novel Homozygous ASNS Mutation and Expanded Phenotype.

Authors:  Jun Sun; Angela J McGillivray; Jason Pinner; Zhihui Yan; Fengxia Liu; Drago Bratkovic; Elizabeth Thompson; Xiuxiu Wei; Huifeng Jiang; Maya Chopra
Journal:  JIMD Rep       Date:  2016-07-27

Review 9.  Report of four novel variants in ASNS causing asparagine synthetase deficiency and review of literature.

Authors:  Chelna Galada; Malavika Hebbar; Leslie Lewis; Santosh Soans; Rajagopal Kadavigere; Anshika Srivastava; Stephanie Bielas; Katta M Girisha; Anju Shukla
Journal:  Congenit Anom (Kyoto)       Date:  2018-02-20       Impact factor: 1.409

10.  Hyperekplexia, microcephaly and simplified gyral pattern caused by novel ASNS mutations, case report.

Authors:  Mohammed Zain Seidahmed; Mustafa A Salih; Omer B Abdulbasit; Abdulmohsen Samadi; Khalid Al Hussien; Abeer M Miqdad; Maha S Biary; Anas M Alazami; Ibrahim A Alorainy; Mohammad M Kabiraj; Ranad Shaheen; Fowzan S Alkuraya
Journal:  BMC Neurol       Date:  2016-07-15       Impact factor: 2.474

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