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Ghosal Hematodiaphyseal Dysplasia: A Case Report
Ghosal hematodiaphyseal dysplasia (GHDD) is a rare autosomal recessive disorder presenting with steroid-responsive anemia and diaphyseal dysplasia of long bones. We report a 3-year-old Iranian girl with refractory anemia, splenomegaly and radiologic signs of metadiaphyseal dysplasia in long bones. T...
Autores principales: | Shakiba, Marjan, Shamsian, Shahin, Malekzadeh, Hamid, Yasaei, Mehrdad |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7231795/ https://www.ncbi.nlm.nih.gov/pubmed/32461797 |
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