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Pediatric Hematology and Oncology Volume 38, 2021 - Issue 6
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Letter

Delayed diagnosis of Griscelli syndrome type 2 with compound heterozygote RAB27A variants presenting with pulmonary failure

Yoav H. Messingera Pediatric Hematology/Oncology, Cancer and Blood Disorders, Children’s Minnesota, Minneapolis, Minnesota, USACorrespondence[email protected]
ORCID Iconhttps://orcid.org/0000-0001-7990-1802View further author information
ORCID Icon,
Tamara C. Pozosb Department of Immunology, Children’s Minnesota, Minneapolis, Minnesota, USAORCID Iconhttps://orcid.org/0000-0003-0763-8763View further author information
ORCID Icon,
Anne G. Griffithsc Children’s Respiratory and Critical Care, Children’sMinnesota, Minneapolis, Minnesota, USAView further author information
,
William A. Mized Department of Radiology, Children’s Minnesota, Minneapolis, Minnesota, USAView further author information
,
Damon R. Olsone Pathology and Laboratory Medicine, Children’s Minnesota, Minneapolis, Minnesota, USAORCID Iconhttps://orcid.org/0000-0001-9727-569XView further author information
ORCID Icon &
Angela R. Smithf University of Minnesota Pediatric Blood and Marrow Transplantation/Cellular Therapy, University of Minnesota, Minneapolis, Minnesota, USAView further author information
Pages 593-601 | Received 04 Nov 2020, Accepted 21 Feb 2021, Published online: 01 Apr 2021
 
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Acknowledgments

The authors acknowledge the patient and her family who were willing to share this information with the public. The authors also acknowledge the insightful comments of the reviewers which have improved the manuscript.

Disclosure statement

The authors declare no conflict of interest.

Consent

Children’s Minnesota Investigation Review Board found the publication of this case report exempt from review, requirement for consent or HIPAA requirement. The patient and mother expressed agreement for this publication.

Additional information

Funding

No outside funding was used for this research.

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