Literature DB >> 22451160

4H syndrome with late-onset growth hormone deficiency caused by POLR3A mutations.

Ana Potic1, Bernard Brais, Karine Choquet, Raphael Schiffmann, Geneviève Bernard.   

Abstract

OBJECTIVE: To report a novel clinical and genetic presentation of a patient with 4H syndrome, which is a recently described leukodystrophy syndrome characterized by ataxia, hypomyelination, hypodontia, and hypogonadotropic hypogonadism.
DESIGN: Case report.
SETTING: University teaching hospital. PATIENT: A 20-year-old male patient with 4H syndrome.
RESULTS: The patient was found to have delayed tooth eruption and a late-onset growth hormone deficiency without overt growth failure. He was a compound heterozygote for the novel missense mutations R1005H and A1331T of POLR3A, which codes for the largest subunit of RNA polymerase III.
CONCLUSION: This is the first report of this type of leukodystrophy from southeastern Europe, which suggests that POLR3A mutations should be suspected in patients with hypomyelination and various central nervous system–based endocrine abnormalities.

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Year:  2012        PMID: 22451160     DOI: 10.1001/archneurol.2011.1963

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  24 in total

1.  Structure of human RNA polymerase III.

Authors:  Ewan Phillip Ramsay; Guillermo Abascal-Palacios; Julia L Daiß; Helen King; Jerome Gouge; Michael Pilsl; Fabienne Beuron; Edward Morris; Philip Gunkel; Christoph Engel; Alessandro Vannini
Journal:  Nat Commun       Date:  2020-12-17       Impact factor: 14.919

2.  Cerebellar hypoplasia with endosteal sclerosis is a POLR3-related disorder.

Authors:  Jamal Ghoumid; Florence Petit; Odile Boute-Benejean; Frédéric Frenois; Maryse Cartigny; Clémence Vanlerberghe; Thomas Smol; Roseline Caumes; Nicolas de Roux; Sylvie Manouvrier-Hanu
Journal:  Eur J Hum Genet       Date:  2017-06-07       Impact factor: 4.246

3.  Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia.

Authors:  Martina Minnerop; Delia Kurzwelly; Holger Wagner; Anne S Soehn; Jennifer Reichbauer; Feifei Tao; Tim W Rattay; Michael Peitz; Kristina Rehbach; Alejandro Giorgetti; Angela Pyle; Holger Thiele; Janine Altmüller; Dagmar Timmann; Ilker Karaca; Martina Lennarz; Jonathan Baets; Holger Hengel; Matthis Synofzik; Burcu Atasu; Shawna Feely; Marina Kennerson; Claudia Stendel; Tobias Lindig; Michael A Gonzalez; Rüdiger Stirnberg; Marc Sturm; Sandra Roeske; Johanna Jung; Peter Bauer; Ebba Lohmann; Stefan Herms; Stefanie Heilmann-Heimbach; Garth Nicholson; Muhammad Mahanjah; Rajech Sharkia; Paolo Carloni; Oliver Brüstle; Thomas Klopstock; Katherine D Mathews; Michael E Shy; Peter de Jonghe; Patrick F Chinnery; Rita Horvath; Jürgen Kohlhase; Ina Schmitt; Michael Wolf; Susanne Greschus; Katrin Amunts; Wolfgang Maier; Ludger Schöls; Peter Nürnberg; Stephan Zuchner; Thomas Klockgether; Alfredo Ramirez; Rebecca Schüle
Journal:  Brain       Date:  2017-06-01       Impact factor: 13.501

Review 4.  RNA Polymerases I and III in development and disease.

Authors:  Kristin En Watt; Julia Macintosh; Geneviève Bernard; Paul A Trainor
Journal:  Semin Cell Dev Biol       Date:  2022-04-11       Impact factor: 7.499

Review 5.  Transcription termination by the eukaryotic RNA polymerase III.

Authors:  Aneeshkumar G Arimbasseri; Keshab Rijal; Richard J Maraia
Journal:  Biochim Biophys Acta       Date:  2012-10-23

6.  More than hypomyelination in Pol-III disorder.

Authors:  Adeline Vanderver; Davide Tonduti; Genevieve Bernard; Jinping Lai; Christopher Rossi; Giovanni Carosso; Martha Quezado; Kondi Wong; Raphael Schiffmann
Journal:  J Neuropathol Exp Neurol       Date:  2013-01       Impact factor: 3.685

Review 7.  Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.

Authors:  Qing Fang; Akima S George; Michelle L Brinkmeier; Amanda H Mortensen; Peter Gergics; Leonard Y M Cheung; Alexandre Z Daly; Adnan Ajmal; María Ines Pérez Millán; A Bilge Ozel; Jacob O Kitzman; Ryan E Mills; Jun Z Li; Sally A Camper
Journal:  Endocr Rev       Date:  2016-11-09       Impact factor: 19.871

Review 8.  RNA Polymerase III Advances: Structural and tRNA Functional Views.

Authors:  Aneeshkumar G Arimbasseri; Richard J Maraia
Journal:  Trends Biochem Sci       Date:  2016-04-08       Impact factor: 13.807

9.  Endocrine Aspects of 4H Leukodystrophy: A Case Report and Review of the Literature.

Authors:  Emma Billington; Geneviève Bernard; William Gibson; Bernard Corenblum
Journal:  Case Rep Endocrinol       Date:  2015-05-31

10.  Dystonia in RNA Polymerase III-Related Leukodystrophy.

Authors:  Ghalia Al Yazidi; Luan T Tran; Kether Guerrero; Adeline Vanderver; Raphael Schiffmann; Nicole I Wolf; Sylvain Chouinard; Geneviève Bernard
Journal:  Mov Disord Clin Pract       Date:  2019-01-09
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