Turner-like Syndrome: a case report
Authors
M.R. Velletri – articles in this journal
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Dipartimento di Pediatria, Università di Messina, Messina, Italy.
M. Valenzise – articles in this journal
Dipartimento di Pediatria, Università di Messina, Messina, Italy.
M. Wasniewska – articles in this journal
Dipartimento di Pediatria, Università di Messina, Messina, Italy.
S. Arasi – articles in this journal
Dipartimento di Pediatria, Università di Messina, Messina, Italy.
A. Santisi – articles in this journal
Dipartimento di Pediatria, Università di Messina, Messina, Italy.
M. Romeo – articles in this journal
Dipartimento di Pediatria, Università di Messina, Messina, Italy.
E. Pitrolo – articles in this journal
Dipartimento di Pediatria, Università di Messina, Messina, Italy.
S. Santucci – articles in this journal
Dipartimento di Pediatria, Università di Messina, Messina, Italy.
D. Corica – articles in this journal
Dipartimento di Pediatria, Università di Messina, Messina, Italy.
R. Crisafulli – articles in this journal
Dipartimento di Pediatria, Università di Messina, Messina, Italy.
G. Zirilli – articles in this journal
Dipartimento di Pediatria, Università di Messina, Messina, Italy.
Published
31 October 2013
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Articles
Abstract
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Abstract
A prepubescent 11 year-old girl came to our attention for short stature. Auxological evaluation showed peculiar phenotype. In order to exclude Turner syndrome standard karyotype was performed with normal result. Because of anemia and selective deficiency of the erythroid lineage further investigations were performed and a diagnosis of Blackfan-Diamond anemia was made.
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Article history
Received: 17 November 2014
Accepted: 17 November 2014
Published: 31 October 2013
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