Literature DB >> 17874088

The neuroradiological findings in a case of Revesz syndrome.

Meir H Scheinfeld1, Yvonne W Lui, Edward A Kolb, Harry M Engel, William A Gomes, Karen M Weidenheim, Jacqueline A Bello.   

Abstract

Revesz syndrome is a variant of dyskeratosis congenita characterized by aplastic anemia, retinopathy, and central nervous system abnormalities. We describe a 3-year-old boy in whom the spectrum of neuroimaging findings, including intracranial calcifications, cerebellar hypoplasia and unusual brain lesions were found by biopsy to be gliosis despite their enhancement and progression. In patients with dyskeratosis-related syndromes, non-neoplastic parenchymal brain lesions occur and gliosis should be considered in the differential diagnosis for progressive enhancing brain lesions. Should this finding be confirmed consistently in additional cases, brain biopsy could potentially be avoided.

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Year:  2007        PMID: 17874088     DOI: 10.1007/s00247-007-0592-0

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN: 0301-0449


  8 in total

Review 1.  Review: coats disease: the 2001 LuEsther T. Mertz lecture.

Authors:  Jerry A Shields; Carol L Shields
Journal:  Retina       Date:  2002-02       Impact factor: 4.256

Review 2.  Dyskeratosis congenita: its link to telomerase and aplastic anaemia.

Authors:  Inderjeet Dokal; Tom Vulliamy
Journal:  Blood Rev       Date:  2003-12       Impact factor: 8.250

Review 3.  Fanconi's anaemia and related bone marrow failure syndromes.

Authors:  Inderjeet Dokal
Journal:  Br Med Bull       Date:  2006-09-11       Impact factor: 4.291

4.  An unusual case of dyskeratosis congenita with intracranial calcifications.

Authors:  P A Duprey; J W Steger
Journal:  J Am Acad Dermatol       Date:  1988-10       Impact factor: 11.527

5.  Gene structure and expression of the mouse dyskeratosis congenita gene, dkc1.

Authors:  N S Heiss; D Bächner; R Salowsky; A Kolb; P Kioschis; A Poustka
Journal:  Genomics       Date:  2000-07-15       Impact factor: 5.736

6.  Association of the congenital bone marrow failure syndromes with retinopathy, intracerebral calcification and progressive neurological impairment.

Authors:  N A Gayatri; M I Hughes; I C Lloyd; R F Wynn
Journal:  Eur J Paediatr Neurol       Date:  2002       Impact factor: 3.140

7.  Bilateral coats retinopathy associated with aplastic anaemia and mild dyskeratotic signs.

Authors:  P Kajtár; K Méhes
Journal:  Am J Med Genet       Date:  1994-02-15

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

  8 in total
  5 in total

1.  Hoyeraal-Hreidarsson syndrome: magnetic resonance imaging findings.

Authors:  Shigeko Kuwashima
Journal:  Jpn J Radiol       Date:  2009-10-27       Impact factor: 2.374

2.  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

Review 3.  Telomeres in aging and disease: lessons from zebrafish.

Authors:  Madalena C Carneiro; Inês Pimenta de Castro; Miguel Godinho Ferreira
Journal:  Dis Model Mech       Date:  2016-07-01       Impact factor: 5.758

Review 4.  Cell biology of disease: Telomeropathies: an emerging spectrum disorder.

Authors:  Brody Holohan; Woodring E Wright; Jerry W Shay
Journal:  J Cell Biol       Date:  2014-05-12       Impact factor: 10.539

Review 5.  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

  5 in total

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