Severe erythroid hypoplasia and erythroblast vacuolization in a male with Brown–Vialetto–Van Laere syndrome 2 misdiagnosed as Diamond Blackfan anemia-Reference-Cited by-同舟云学术

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Severe erythroid hypoplasia and erythroblast vacuolization in a male with Brown–Vialetto–Van Laere syndrome 2 misdiagnosed as Diamond Blackfan anemia

Published:2023-05-02 Issue:10 Volume:70 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Chen Yanxia¹,Zhao Jiwei²,McLinden A. Patrick³,Luo Meizhu⁴,Cao Ke⁴,Liu Jinlin⁵^ORCID

Affiliation:

1. Department of Rheumatology and Immunology, South China Hospital, Medical School Shenzhen University Shenzhen Guangdong China

2. Department of Laboratory Medicine Nanjing Lishui District Hospital of TraditionalChinese Medicine Nanjing Jiangsu China

3. Division of Pulmonary and Critical Care Medicine University of Michigan Health System Ann Arbor Michigan USA

4. Clinical Laboratory Shenzhen Children's Hospital Shenzhen Guangdong China

5. Department of Clinical Laboratory, South China Hospital, Medical School Shenzhen University Shenzhen Guangdong China

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.30396

Reference7 articles.

1. Thirteen‐month‐old girl with hyporegenerative macrocytic anemia due to Brown–Vialetto–Van Laere syndrome 2

2. First report of paternal uniparental disomy of chromosome 8 with SLC52A2 mutation in Brown-vialetto-van laere syndrome type 2 and an analysis of genotype-phenotype correlations

3. Riboflavin in Neurological Diseases: A Narrative Review

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