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Fanconi Syndrome | 76877

Journal du rein

ISSN - 2472-1220

Abstrait

Fanconi Syndrome

Harika Yasam

Fanconi anemia is a rare genetic disorder, involving all three blood cell lines. It is the most common cause of inherited bone marrow failure characterized by the pancytopenia. This activity reviews the evaluation and management of Fanconi anemia and highlights the role of the interprofessional team in improving care for patients with this condition.

Identify the etiology of Fanconi anemia. Describe the appropriate evaluation of Fanconi anemia. Outline the management options available for Fanconi anemia. Summarize interprofessional team strategies for improving care coordination and communication to advance the care of Fanconi anemia and improve outcomes.

Avertissement: Ce résumé a été traduit à l'aide d'outils d'intelligence artificielle et n'a pas encore été examiné ni vérifié