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fanconi anemia/edema
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4 resultados
Naso-orbicular tissue necrosis by Streptococcus parasanguis in a patient with Fanconi anemia: clinical and laboratory aspects.
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Fanconi anemia (FA) is a rare autosomal recessive disorder, characterized by pancytopenia and progressive hypoplasia of the bone marrow. A 23-year-old woman with FA showed severe pancytopenia and developed an abscess on the infraorbicular region on the right side of the face that progressed to
Hyperbaric oxygen should not be used in the management of hemorrhagic cystitis in patients with Fanconi anemia.
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Hemorrhagic cystitis (HC) is a common complication after stem cell transplantation (SCT) that occurs more frequently in patients with Fanconi anemia (FA) because of hypersensitivity of their cells to the agents used in the preparation for SCT (chemo and radiation). Many HC cases respond to therapy
Postoperative clinical radiosensitivity in patients with fanconi anemia and head and neck squamous cell carcinoma.
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OBJECTIVE
To describe the complications and adverse effects of postoperative radiotherapy in patients with Fanconi anemia (FA).
METHODS
Cohort study.
METHODS
Patients with FA treated at community and tertiary care hospitals throughout the United States.
METHODS
The study included patients with FA
The zebrafish kidney mutant zeppelin reveals that brca2/fancd1 is essential for pronephros development.
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The zebrafish kidney is conserved with other vertebrates, making it an excellent genetic model to study renal development. The kidney collects metabolic waste using a blood filter with specialized epithelial cells known as podocytes. Podocyte formation is poorly understood but relevant to many
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