Literature DB >> 33341249

Molecular Genetics and Modifier Genes in Pseudoxanthoma Elasticum, a Heritable Multisystem Ectopic Mineralization Disorder.

Hongbin Luo1, Masoomeh Faghankhani2, Yi Cao3, Jouni Uitto4, Qiaoli Li5.   

Abstract

In the past two decades, there has been great progress in identifying the molecular basis and pathomechanistic details in pseudoxanthoma elasticum (PXE), a heritable multisystem ectopic mineralization disorder. Although the identification of pathogenic variants in ABCC6 has been critical for understanding the disease process, genetic modifiers have been disclosed that explain the phenotypic heterogeneity of PXE. Adding to the genetic complexity of PXE are PXE-like phenotypes caused by pathogenic variants in other ectopic mineralization-associated genes. This review summarizes the current knowledge of the genetics and candidate modifier genes in PXE, a multifactorial disease at the genome-environment interface.
Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.

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Year:  2020        PMID: 33341249      PMCID: PMC8068569          DOI: 10.1016/j.jid.2020.10.013

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  119 in total

1.  Mutations in ABCC6 cause pseudoxanthoma elasticum.

Authors:  A A Bergen; A S Plomp; E J Schuurman; S Terry; M Breuning; H Dauwerse; J Swart; M Kool; S van Soest; F Baas; J B ten Brink; P T de Jong
Journal:  Nat Genet       Date:  2000-06       Impact factor: 38.330

2.  Recessive mutations in the gene encoding the tight junction protein occludin cause band-like calcification with simplified gyration and polymicrogyria.

Authors:  Mary C O'Driscoll; Sarah B Daly; Jill E Urquhart; Graeme C M Black; Daniela T Pilz; Knut Brockmann; Meriel McEntagart; Ghada Abdel-Salam; Maha Zaki; Nicole I Wolf; Roger L Ladda; Susan Sell; Stefano D'Arrigo; Waney Squier; William B Dobyns; John H Livingston; Yanick J Crow
Journal:  Am J Hum Genet       Date:  2010-08-19       Impact factor: 11.025

3.  Pseudoxanthoma elasticum: a streamlined, ethnicity-based mutation detection strategy.

Authors:  Jennifer Larusso; Franziska Ringpfeil; Jouni Uitto
Journal:  Clin Transl Sci       Date:  2010-12       Impact factor: 4.689

4.  A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts.

Authors:  Ganeshwaran H Mochida; Vijay S Ganesh; Jillian M Felie; Danielle Gleason; R Sean Hill; Katie Rose Clapham; Daniel Rakiec; Wen-Hann Tan; Nadia Akawi; Muna Al-Saffar; Jennifer N Partlow; Sigrid Tinschert; A James Barkovich; Bassam Ali; Lihadh Al-Gazali; Christopher A Walsh
Journal:  Am J Hum Genet       Date:  2010-11-25       Impact factor: 11.025

5.  Autosomal recessive HEM/Greenberg skeletal dysplasia is caused by 3 beta-hydroxysterol delta 14-reductase deficiency due to mutations in the lamin B receptor gene.

Authors:  Hans R Waterham; Janet Koster; Petra Mooyer; Gerard van Noort Gv; Richard I Kelley; William R Wilcox; Ronald J A Wanders; Raoul C M Hennekam; Jan C Oosterwijk
Journal:  Am J Hum Genet       Date:  2003-02-28       Impact factor: 11.025

6.  Hypophosphatemia, hyperphosphaturia, and bisphosphonate treatment are associated with survival beyond infancy in generalized arterial calcification of infancy.

Authors:  Frank Rutsch; Petra Böyer; Yvonne Nitschke; Nico Ruf; Bettina Lorenz-Depierieux; Tanja Wittkampf; Gabriele Weissen-Plenz; Rudolf-Josef Fischer; Zulf Mughal; John W Gregory; Justin H Davies; Chantal Loirat; Tim M Strom; Dirk Schnabel; Peter Nürnberg; Robert Terkeltaub
Journal:  Circ Cardiovasc Genet       Date:  2008-12

7.  Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice.

Authors:  Annika Keller; Ana Westenberger; Maria J Sobrido; Maria García-Murias; Aloysius Domingo; Renee L Sears; Roberta R Lemos; Andres Ordoñez-Ugalde; Gael Nicolas; José E Gomes da Cunha; Elisabeth J Rushing; Michael Hugelshofer; Moritz C Wurnig; Andres Kaech; Regina Reimann; Katja Lohmann; Valerija Dobričić; Angel Carracedo; Igor Petrović; Janis M Miyasaki; Irina Abakumova; Maarja Andaloussi Mäe; Elisabeth Raschperger; Mayana Zatz; Katja Zschiedrich; Jörg Klepper; Elizabeth Spiteri; Jose M Prieto; Inmaculada Navas; Michael Preuss; Carmen Dering; Milena Janković; Martin Paucar; Per Svenningsson; Kioomars Saliminejad; Hamid R K Khorshid; Ivana Novaković; Adriano Aguzzi; Andreas Boss; Isabelle Le Ber; Gilles Defer; Didier Hannequin; Vladimir S Kostić; Dominique Campion; Daniel H Geschwind; Giovanni Coppola; Christer Betsholtz; Christine Klein; Joao R M Oliveira
Journal:  Nat Genet       Date:  2013-08-04       Impact factor: 38.330

Review 8.  Vitamin K-dependent carboxylation.

Authors:  Kathleen L Berkner
Journal:  Vitam Horm       Date:  2008       Impact factor: 3.421

9.  Spectrum of genetic variation at the ABCC6 locus in South Africans: Pseudoxanthoma elasticum patients and healthy individuals.

Authors:  Michèle Ramsay; Tarryn Greenberg; Zane Lombard; Robyn Labrum; Steven Lubbe; Shaun Aron; Anna-Susan Marais; Sharon Terry; Lionel Bercovitch; Denis Viljoen
Journal:  J Dermatol Sci       Date:  2009-03-31       Impact factor: 4.563

10.  Mutations in a gene encoding an ABC transporter cause pseudoxanthoma elasticum.

Authors:  O Le Saux; Z Urban; C Tschuch; K Csiszar; B Bacchelli; D Quaglino; I Pasquali-Ronchetti; F M Pope; A Richards; S Terry; L Bercovitch; A de Paepe; C D Boyd
Journal:  Nat Genet       Date:  2000-06       Impact factor: 38.330

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  7 in total

Review 1.  [Syndroms associated with benign skin tumors].

Authors:  George-Sorin Tiplica; Klaus Fritz; Alexandra Irina Butacu; Loredana Ungureanu; Carmen Maria Sălăvăstru
Journal:  Hautarzt       Date:  2022-01-25       Impact factor: 0.751

2.  Functional Assessment of Missense Variants in the ABCC6 Gene Implicated in Pseudoxanthoma Elasticum, a Heritable Ectopic Mineralization Disorder.

Authors:  Luke Kowal; Jianhe Huang; Hongbin Luo; Jagmohan Singh; Adam E Snook; Jouni Uitto; Qiaoli Li
Journal:  J Invest Dermatol       Date:  2021-09-29       Impact factor: 8.551

Review 3.  Inorganic Pyrophosphate Deficiency Syndromes and Potential Treatments for Pathologic Tissue Calcification.

Authors:  Douglas Ralph; Koen van de Wetering; Jouni Uitto; Qiaoli Li
Journal:  Am J Pathol       Date:  2022-02-16       Impact factor: 5.770

4.  Genetic heterogeneity of heritable ectopic mineralization disorders in a large international cohort.

Authors:  Amir Hossein Saeidian; Leila Youssefian; Jianhe Huang; Andrew Touati; Hassan Vahidnezhad; Luke Kowal; Matthew Caffet; Tamara Wurst; Jagmohan Singh; Adam E Snook; Ellen Ryu; Paolo Fortina; Sharon F Terry; Jonathan G Schoenecker; Jouni Uitto; Qiaoli Li
Journal:  Genet Med       Date:  2021-11-30       Impact factor: 8.864

5.  Comment on "Clinical practice guidelines for pseudoxanthoma elasticum (2017)": The importance of mutation analysis.

Authors:  Qiaoli Li; Sharon F Terry; Jouni Uitto
Journal:  J Dermatol       Date:  2022-03-22       Impact factor: 3.468

Review 6.  Mutation update: Variants of the ENPP1 gene in pathologic calcification, hypophosphatemic rickets, and cutaneous hypopigmentation with punctate keratoderma.

Authors:  Douglas Ralph; Michael A Levine; Gabriele Richard; Michelle M Morrow; Elizabeth K Flynn; Jouni Uitto; Qiaoli Li
Journal:  Hum Mutat       Date:  2022-05-18       Impact factor: 4.700

7.  ENPP1 variants in patients with GACI and PXE expand the clinical and genetic heterogeneity of heritable disorders of ectopic calcification.

Authors:  Douglas Ralph; Yvonne Nitschke; Michael A Levine; Matthew Caffet; Tamara Wurst; Amir Hossein Saeidian; Leila Youssefian; Hassan Vahidnezhad; Sharon F Terry; Frank Rutsch; Jouni Uitto; Qiaoli Li
Journal:  PLoS Genet       Date:  2022-04-28       Impact factor: 5.917

  7 in total

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