Open AccessScapula alata as presenting symptom of Fanconi anemia: A case for serendipity
Author(s) -
Adrichem Renee,
Weger Vincent,
Broere Daniel,
Herrewegen Femke,
Amaya Jeremy,
ten Tusscher Gavin William
Publication year - 2019
Publication title -
clinical case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.21
H-Index - 9
ISSN - 2050-0904
DOI - 10.1002/ccr3.2323
Subject(s) - medicine , fanconi anemia , scapula , genetic disorder , anemia , serendipity , dermatology , pathology , genetics , anatomy , disease , dna , biology , dna repair , philosophy , epistemology
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.