Literature DB >> 31889758

Mutation in the Neuroblastoma Amplified Sequence Gene as a Cause of Recurrent Acute Liver Failure, Acute Kidney Injury, and Status Epilepticus.

Snehal Mallakmir1, Aabha Nagral2, Abhijit Bagde3, Darius Mirza4,5, Rashid Merchant6, Vijay Yewale7.   

Abstract

Cause of acute liver failure (ALF) in children remains elusive in almost 50% cases. It is caused by viral hepatitis, hemophagocytic lymphohistiocytosis, autoimmune diseases, drugs, and metabolic diseases. Recurrent ALF with intermittent recovery is caused by metabolic disorders such as fatty acid oxidation defects, respiratory chain disorders, or unknown repeat insult from diet, toxins, or viruses. Biallelic mutations in the neuroblastoma amplified sequence (NBAS) gene have recently been associated with infantile liver failure syndrome type 2. It is associated with ALF during intercurrent febrile illness and complete recovery with conservative management. A 12-year-old boy presented with history of recurrent ALF since infancy with complete recovery and no etiological clue. He was detected to have homozygous pathogenic variation in NBAS gene which has been recently described in the literature to be associated with recurrent ALF. This is the first such case report from India. During the episode of ALF, when he presented to us, he had acute kidney injury and status epilepticus. The association of other organs with NBAS protein deficiency-associated ALF needs to be established.
© 2019 Indian National Association for Study of the Liver. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  ALF; NBAS; infantile acute liver failure syndrome 2

Year:  2019        PMID: 31889758      PMCID: PMC6926219          DOI: 10.1016/j.jceh.2019.03.008

Source DB:  PubMed          Journal:  J Clin Exp Hepatol        ISSN: 0973-6883


  8 in total

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Authors:  Antal Dezsőfi; Ulrich Baumann; Anil Dhawan; Ozlem Durmaz; Björn Fischler; Nedim Hadzic; Loreto Hierro; Florence Lacaille; Valérie A McLin; Valerio Nobili; Piotr Socha; Pietro Vajro; Alexander S Knisely
Journal:  J Pediatr Gastroenterol Nutr       Date:  2015-03       Impact factor: 2.839

4.  Pattern of diagnostic evaluation for the causes of pediatric acute liver failure: an opportunity for quality improvement.

Authors:  Michael R Narkewicz; Dominic Dell Olio; Saul J Karpen; Karen F Murray; Kathy Schwarz; Nada Yazigi; Song Zhang; Steven H Belle; Robert H Squires
Journal:  J Pediatr       Date:  2009-07-29       Impact factor: 4.406

Review 5.  Clinical approach to inherited metabolic disorders in neonates: an overview.

Authors:  J M Saudubray; M C Nassogne; P de Lonlay; G Touati
Journal:  Semin Neonatol       Date:  2002-02

6.  Neuroblastoma amplified sequence gene is associated with a novel short stature syndrome characterised by optic nerve atrophy and Pelger-Huët anomaly.

Authors:  Nadezda Maksimova; Kenju Hara; Irina Nikolaeva; Tan Chun-Feng; Tomoaki Usui; Mineo Takagi; Yasushi Nishihira; Akinori Miyashita; Hiroshi Fujiwara; Tokuhide Oyama; Anna Nogovicina; Aitalina Sukhomyasova; Svetlana Potapova; Ryozo Kuwano; Hitoshi Takahashi; Masatoyo Nishizawa; Osamu Onodera
Journal:  J Med Genet       Date:  2010-06-24       Impact factor: 6.318

7.  Biallelic Mutations in NBAS Cause Recurrent Acute Liver Failure with Onset in Infancy.

Authors:  Tobias B Haack; Christian Staufner; Marlies G Köpke; Beate K Straub; Stefan Kölker; Christian Thiel; Peter Freisinger; Ivo Baric; Patrick J McKiernan; Nicola Dikow; Inga Harting; Flemming Beisse; Peter Burgard; Urania Kotzaeridou; Joachim Kühr; Urban Himbert; Robert W Taylor; Felix Distelmaier; Jerry Vockley; Lina Ghaloul-Gonzalez; Johannes Zschocke; Laura S Kremer; Elisabeth Graf; Thomas Schwarzmayr; Daniel M Bader; Julien Gagneur; Thomas Wieland; Caterina Terrile; Tim M Strom; Thomas Meitinger; Georg F Hoffmann; Holger Prokisch
Journal:  Am J Hum Genet       Date:  2015-06-11       Impact factor: 11.025

8.  NBAS mutations cause acute liver failure: when acetaminophen is not a culprit.

Authors:  Pier Luigi Calvo; Francesco Tandoi; Tobias B Haak; Andrea Brunati; Michele Pinon; Dominic Dell Olio; Renato Romagnoli; Marco Spada
Journal:  Ital J Pediatr       Date:  2017-09-25       Impact factor: 2.638

  8 in total

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