Literature DB >> 1404302

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

T Revesz1, S Fletcher, L I al-Gazali, P DeBuse.   

Abstract

A male infant was found to have bilateral exudative retinopathy at 6 months of age. A month later severe aplastic anaemia was diagnosed, eventually leading to the infant's death. Additional features of this seemingly new syndrome were intrauterine growth retardation, fine sparse hair, fine reticulate skin pigmentation, ataxia because of cerebellar hypoplasia, cerebral calcifications, extensor hypertonia, and progressive psychomotor retardation.

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Year:  1992        PMID: 1404302      PMCID: PMC1016105          DOI: 10.1136/jmg.29.9.673

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  4 in total

1.  A familial syndrome with coats' reaction retinal angiomas, hair and nail defects and intracranial calcification.

Authors:  J L Tolmie; B H Browne; P M McGettrick; J B Stephenson
Journal:  Eye (Lond)       Date:  1988       Impact factor: 3.775

2.  Dyskeratosis congenita.

Authors:  H R Davidson; J M Connor
Journal:  J Med Genet       Date:  1988-12       Impact factor: 6.318

Review 3.  Dyskeratosis congenita: clinical features and genetic aspects. Report of a family and review of the literature.

Authors:  C Sirinavin; A A Trowbridge
Journal:  J Med Genet       Date:  1975-12       Impact factor: 6.318

4.  Dyskeratosis congenita with hypoplastic anemia: a stem cell defect.

Authors:  M Friedland; J D Lutton; R Spitzer; R D Levere
Journal:  Am J Hematol       Date:  1985-09       Impact factor: 10.047

  4 in total
  32 in total

Review 1.  The molecular genetics of the telomere biology disorders.

Authors:  Alison A Bertuch
Journal:  RNA Biol       Date:  2015-09-23       Impact factor: 4.652

2.  Revesz syndrome.

Authors:  A Riyaz; Najeeba Riyaz; M P Jayakrishnan; P T Mohamed Shiras; V T Ajith Kumar; Bindu S Ajith
Journal:  Indian J Pediatr       Date:  2007-09       Impact factor: 1.967

3.  Dyskeratosis congenita caused by a novel TERT point mutation in siblings with pancytopenia and exudative retinopathy.

Authors:  Akshay Sharma; Kasiani Myers; Zhan Ye; John D'Orazio
Journal:  Pediatr Blood Cancer       Date:  2014-07-25       Impact factor: 3.167

4.  Genetic Variations in Telomere Maintenance, with Implications on Tissue Renewal Capacity and Chronic Disease Pathologies.

Authors:  M A Trudeau; J M Y Wong
Journal:  Curr Pharmacogenomics Person Med       Date:  2010-03-01

Review 5.  Dyskeratosis congenita as a disorder of telomere maintenance.

Authors:  Nya D Nelson; Alison A Bertuch
Journal:  Mutat Res       Date:  2011-07-02       Impact factor: 2.433

6.  The neuroradiological findings in a case of Revesz syndrome.

Authors:  Meir H Scheinfeld; Yvonne W Lui; Edward A Kolb; Harry M Engel; William A Gomes; Karen M Weidenheim; Jacqueline A Bello
Journal:  Pediatr Radiol       Date:  2007-09-14

7.  PERIPHERAL RETINOPATHY ASSOCIATED WITH APLASTIC ANEMIA.

Authors:  Tatyana I Metelitsina; Veeral S Sheth; Shuchi B Patel; Michael A Grassi
Journal:  Retin Cases Brief Rep       Date:  2017 Spring

Review 8.  The role of telomere biology in bone marrow failure and other disorders.

Authors:  Sharon A Savage; Blanche P Alter
Journal:  Mech Ageing Dev       Date:  2007-11-19       Impact factor: 5.432

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

Authors:  Michael J Allingham
Journal:  Ophthalmic Surg Lasers Imaging Retina       Date:  2016-04-01       Impact factor: 1.300

10.  Leukoencephalopathy, cerebral calcifications and cysts: a family study.

Authors:  Kinga Karlinger; Ádám Domonkos Tárnoki; Dávid László Tárnoki; Anne Polvi; Anna-Elina Lehesjoki; Andrea Kelemen; László Szegedi; Eszter Turányi; Anita Kamondi; Anna Szűcs
Journal:  J Neurol       Date:  2014-07-18       Impact factor: 4.849

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