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BMJ Case Reports 2018; doi:10.1136/bcr-2018-224477
  • Images in…

Retinopathy and bone marrow failure revealing Coats plus syndrome

  1. Sara Batalha3
  1. 1Paediatrics Department, Hospital Dona Estefania, CHLC, Lisbon, Portugal
  2. 2Neuroradiology Department, Hospital de São José, CHLC, Lisbon, Portugal
  3. 3Paediatric Haematology Department, Hospital Dona Estefania, CHLC, Lisbon, Portugal
  1. Correspondence to Dr Teresa Painho, maria.teresa.painho{at}gmail.com
  • Accepted 18 February 2018
  • Published 9 March 2018

Description

The inherited bone marrow failure syndromes (IBMFS) are a group of clinically heterogeneous disorders in which at least one hematopoietic cell lineage is significantly reduced in number.1 Dyskeratosis congenita (DC), an IBMFS caused by germline defects in telomere biology, is diagnosed by the presence of the classic clinical triad of nail dysplasia, lacy skin pigmentation and oral leukoplakia. There are clinical variants of DC, namely Hoyeraal-Hreidarsson syndrome, Revesz syndrome, and Coats plus syndrome (CpS) or cerebroretinal microangiopathy with calcification and cysts.2 CpS is a very rare disorder in which the most characteristic features are: retinal telangiectasia and exudates (Coats disease); distinctive pattern of intracranial calcification with …

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