Literature DB >> 27065378

Bilateral Proliferative Retinopathy Associated With Hoyeraal-Hreidarsson Syndrome, a Severe Form of Dyskeratosis Congenita.

Michael J Allingham.   

Abstract

Dyskeratosis congenita (DC) is the prototypical member of a family of diseases caused by defective telomere maintenance. These "telomeropathies" also include Hoyeraal-Hreidarsson syndrome (HH) and Revesz syndrome, which are severe forms of dyskeratosis congenita, as well as a subset of idiopathic pulmonary fibrosis, aplastic anemia, and Coats' plus syndrome. Retinopathy has only rarely been reported in DC and HH, but is universally present in Coats' plus and Revesz syndromes. The care of these patients is typically a multidisciplinary effort, and this should include monitoring by an ophthalmologist. Copyright 2016, SLACK Incorporated.

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Year:  2016        PMID: 27065378      PMCID: PMC5217527          DOI: 10.3928/23258160-20160324-11

Source DB:  PubMed          Journal:  Ophthalmic Surg Lasers Imaging Retina        ISSN: 2325-8160            Impact factor:   1.300


  10 in total

Review 1.  Dyskeratosis congenita.

Authors:  Inderjeet Dokal
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2011

2.  Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus.

Authors:  Beverley H Anderson; Paul R Kasher; Josephine Mayer; Marcin Szynkiewicz; Emma M Jenkinson; Sanjeev S Bhaskar; Jill E Urquhart; Sarah B Daly; Jonathan E Dickerson; James O'Sullivan; Elisabeth Oppliger Leibundgut; Joanne Muter; Ghada M H Abdel-Salem; Riyana Babul-Hirji; Peter Baxter; Andrea Berger; Luisa Bonafé; Janice E Brunstom-Hernandez; Johannes A Buckard; David Chitayat; Wui K Chong; Duccio M Cordelli; Patrick Ferreira; Joel Fluss; Ewan H Forrest; Emilio Franzoni; Caterina Garone; Simon R Hammans; Gunnar Houge; Imelda Hughes; Sebastien Jacquemont; Pierre-Yves Jeannet; Rosalind J Jefferson; Ram Kumar; Georg Kutschke; Staffan Lundberg; Charles M Lourenço; Ramesh Mehta; Sakkubai Naidu; Ken K Nischal; Luís Nunes; Katrin Ounap; Michel Philippart; Prab Prabhakar; Sarah R Risen; Raphael Schiffmann; Calvin Soh; John B P Stephenson; Helen Stewart; Jon Stone; John L Tolmie; Marjo S van der Knaap; Jose P Vieira; Catheline N Vilain; Emma L Wakeling; Vanessa Wermenbol; Andrea Whitney; Simon C Lovell; Stefan Meyer; John H Livingston; Gabriela M Baerlocher; Graeme C M Black; Gillian I Rice; Yanick J Crow
Journal:  Nat Genet       Date:  2012-01-22       Impact factor: 38.330

3.  Bilateral retinal vasculopathy in a patient with dyskeratosis congenita.

Authors:  Luiz F Teixeira; Carol L Shields; Brian Marr; Noel Horgan; Jerry A Shields
Journal:  Arch Ophthalmol       Date:  2008-01

4.  Vitreous hemorrhage secondary to retinal vasculopathy in a patient with dyskeratosis congenita.

Authors:  Alessandro Finzi; Mariachiara Morara; Francesco Pichi; Chiara Veronese; Antonio P Ciardella
Journal:  Int Ophthalmol       Date:  2013-10-10       Impact factor: 2.031

5.  Ocular and orbital manifestations of the inherited bone marrow failure syndromes: Fanconi anemia and dyskeratosis congenita.

Authors:  Ekaterini T Tsilou; Neelam Giri; Sarah Weinstein; Christine Mueller; Sharon A Savage; Blanche P Alter
Journal:  Ophthalmology       Date:  2009-12-22       Impact factor: 12.079

6.  Proliferative retinopathy as a complication of dyskeratosis congenita.

Authors:  John O Mason; Jacob J Yunker; Peter A Nixon; Rachel S Vail; Ekaterina Tsilou; Neelam Giri; Blanche P Alter
Journal:  Retin Cases Brief Rep       Date:  2009

7.  Coats' plus: a progressive familial syndrome of bilateral Coats' disease, characteristic cerebral calcification, leukoencephalopathy, slow pre- and post-natal linear growth and defects of bone marrow and integument.

Authors:  Y J Crow; J McMenamin; C A Haenggeli; D M Hadley; S Tirupathi; E P Treacy; S M Zuberi; B H Browne; J L Tolmie; J B P Stephenson
Journal:  Neuropediatrics       Date:  2004-02       Impact factor: 1.947

8.  Bilateral retinopathy, aplastic anaemia, and central nervous system abnormalities: a new syndrome?

Authors:  T Revesz; S Fletcher; L I al-Gazali; P DeBuse
Journal:  J Med Genet       Date:  1992-09       Impact factor: 6.318

9.  Retinal vasculopathy in a family with autosomal dominant dyskeratosis congenita.

Authors:  Charles A Johnson; Mark Hatfield; Jose S Pulido
Journal:  Ophthalmic Genet       Date:  2009-12       Impact factor: 1.803

10.  Bilateral retinal vasculopathy associated with autosomal dominant dyskeratosis congenita.

Authors:  Sara Vaz-Pereira; Patricio A Pacheco; Shreyans Gandhi; Austin G Kulasekararaj; Judith C Marsh; Bishwanath Pal; Ghulam J Mufti
Journal:  Eur J Ophthalmol       Date:  2013-05-03       Impact factor: 2.597

  10 in total
  2 in total

Review 1.  Ocular findings and genomics of X-linked recessive disorders: A review.

Authors:  Asima Hassan; Yaser R Mir; Raja A H Kuchay
Journal:  Indian J Ophthalmol       Date:  2022-07       Impact factor: 2.969

Review 2.  Revesz syndrome revisited.

Authors:  Michael Karremann; Eva Neumaier-Probst; Frank Schlichtenbrede; Fabian Beier; Tim H Brümmendorf; Friedrich W Cremer; Peter Bader; Matthias Dürken
Journal:  Orphanet J Rare Dis       Date:  2020-10-23       Impact factor: 4.123

  2 in total

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