Shwachman-Diamond syndrome: clinical case
Vol. 21 No. 2 (2017), Pediatric Hematology
Vol. 21 No. 2 (2017)

Shwachman-Diamond syndrome: clinical case

Pediatric Hematology
Published 2019-04-29
P Lagrotta
Hematología Infantil. Hospital Nacional Dr. A. Posadas El Palomar, Buenos Aires, Argentina
E García
Hematología Infantil. Hospital Prof. A. Posadas
ISSN 2250-8309 (versión en línea) - ISSN 0329-0379 (versión impresa)
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Keywords

Shwachman-Diamond syndrome, Neutropenia, Steatorrhea

How to Cite

Lagrotta, P., & García, E. (2019). Shwachman-Diamond syndrome: clinical case. Journal of Hematology, 21(2), 219–221. Retrieved from https://revistahematologia.com.ar/index.php/Revista/article/view/157
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Abstract

Schwachman-Diamond syndrome is a rare, autosomal recessive disease characterized by exocrine pancreatic insufficiency, bone marrow dysfunction, skeletal disorders and low stature. We report an 8 year-old patient who was admitted to Prof. A. Posadas Hospital Hematology Pediatric department because of neutropenia.

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References

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