Scapula alata as presenting symptom of Fanconi anemia: A case for serendipity

Fanconi anemia is a recessive genetic disorder with a wide range of presenting symptoms, from multiple congenital defects to exclusively (pan) cytopenia. Scapula alata may be a rare symptom of FA.

Detalles Bibliográficos
Autores principales: van Adrichem, Renee, de Weger, Vincent, Broere, Daniel, van Herrewegen, Femke, Amaya, Jeremy, ten Tusscher, Gavin William
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745367/
https://www.ncbi.nlm.nih.gov/pubmed/31534721
http://dx.doi.org/10.1002/ccr3.2323
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author van Adrichem, Renee
de Weger, Vincent
Broere, Daniel
van Herrewegen, Femke
Amaya, Jeremy
ten Tusscher, Gavin William
author_facet van Adrichem, Renee
de Weger, Vincent
Broere, Daniel
van Herrewegen, Femke
Amaya, Jeremy
ten Tusscher, Gavin William
author_sort van Adrichem, Renee
collection PubMed
description Fanconi anemia is a recessive genetic disorder with a wide range of presenting symptoms, from multiple congenital defects to exclusively (pan) cytopenia. Scapula alata may be a rare symptom of FA.
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spelling pubmed-67453672019-09-18 Scapula alata as presenting symptom of Fanconi anemia: A case for serendipity van Adrichem, Renee de Weger, Vincent Broere, Daniel van Herrewegen, Femke Amaya, Jeremy ten Tusscher, Gavin William Clin Case Rep Case Reports Fanconi anemia is a recessive genetic disorder with a wide range of presenting symptoms, from multiple congenital defects to exclusively (pan) cytopenia. Scapula alata may be a rare symptom of FA. John Wiley and Sons Inc. 2019-07-23 /pmc/articles/PMC6745367/ /pubmed/31534721 http://dx.doi.org/10.1002/ccr3.2323 Text en © 2019 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Case Reports
van Adrichem, Renee
de Weger, Vincent
Broere, Daniel
van Herrewegen, Femke
Amaya, Jeremy
ten Tusscher, Gavin William
Scapula alata as presenting symptom of Fanconi anemia: A case for serendipity
title Scapula alata as presenting symptom of Fanconi anemia: A case for serendipity
title_full Scapula alata as presenting symptom of Fanconi anemia: A case for serendipity
title_fullStr Scapula alata as presenting symptom of Fanconi anemia: A case for serendipity
title_full_unstemmed Scapula alata as presenting symptom of Fanconi anemia: A case for serendipity
title_short Scapula alata as presenting symptom of Fanconi anemia: A case for serendipity
title_sort scapula alata as presenting symptom of fanconi anemia: a case for serendipity
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745367/
https://www.ncbi.nlm.nih.gov/pubmed/31534721
http://dx.doi.org/10.1002/ccr3.2323
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