Literature DB >> 26808426

Novel VIPAS39 mutation in a syndromic patient with arthrogryposis, renal tubular dysfunction and intrahepatic cholestasis.

Majid Aflatounian1, Holly Smith2, Fatemeh Farahani1, Azam Tofighi Naeem1, Anna Straatman-Iwanowska2, Samaneh Zoghi3, Urvi Khatri2, Parisa Tajdini1, Gholam Hossein Fallahi1, Paul Gissen2, Nima Rezaei4.   

Abstract

ARC syndrome is a rare autosomal recessive disease, characterized by arthrogryposis, renal tubular dysfunction and cholestasis. Herein a 2.5 month old infant with dysmorphic features, including small anterior fontanel, low set ears, beaked nose and high arched palate is presented who was referred because of icterus. He also suffered from some additional anomalies, including unilateral choanal atresia, club foot, and bilateral developmental dislocation of hip, while further studies showed renal tubular acidosis and hearing impairment in addition to cholestasis. Genetic studies showed a homozygous mutation in the VIPAS39 gene. Making the definite diagnosis of the syndrome is important, while increased risk of mutation in other siblings highlights the importance of prenatal diagnosis.
Copyright © 2016 Elsevier Masson SAS. All rights reserved.

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Keywords:  Cholestasis; Mutation; Prenatal diagnosis; Syndrome

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Year:  2016        PMID: 26808426     DOI: 10.1016/j.ejmg.2016.01.005

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  1 in total

1.  FERARI is required for Rab11-dependent endocytic recycling.

Authors:  Jachen A Solinger; Harun-Or Rashid; Cristina Prescianotto-Baschong; Anne Spang
Journal:  Nat Cell Biol       Date:  2020-01-27       Impact factor: 28.824

  1 in total

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