Treatment of congenital erythropoietic porphyria in children by allogeneic stem cell transplantion: A case report and review of the literature

Keyphrases

• Allogeneic Stem Cells 100%
• Erythropoietic Protoporphyria 100%
• Transplantion 100%
• Stem Cell Transplantation 66%
• Erythrodontia 66%
• Uroporphyrinogen III 66%
• Autosomal Recessive 33%
• Transplantation 33%
• Disease Manifestations 33%
• Curative Treatment 33%
• Clinical Experience 33%
• Splenomegaly 33%
• Genetic Defects 33%
• Disease-free 33%
• Stool 33%
• Erythrocytes 33%
• Porphyrin 33%
• Skin Lesions 33%
• Allogeneic Bone Marrow Transplantation 33%
• Long-term Survivors 33%
• Matched Sibling 33%
• Hemolytic Anemia 33%
• HLA-matched Donor 33%
• Child Self-report 33%
• Bone Fragility 33%
• Porphyrin Metabolism 33%
• Uroporphyrin 33%

Medicine and Dentistry

• Diseases 100%
• Erythropoietic Porphyria 100%
• Stem Cell 100%
• Stem Cell Therapy 40%
• Uroporphyrinogen 40%
• Transplantation 20%
• Bone Marrow Transplantation 20%
• Genetic Disorder 20%
• Skin Defect 20%
• Splenomegaly 20%
• Hemolytic Anemia 20%
• Erythrocyte 20%
• Porphyrin 20%
• Uroporphyrin 20%
• Bone Fragility 20%
• Porphyrin Metabolism 20%
• Autosomal Recessive Disorder 20%
• Metabolite 20%
• Photosensitivity 20%