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Drepanocitosis: situación actual y perspectivas
Nursing (Ed Española), 2017 Vincent M. Vacca, Lora Blank
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EMC Pediatria, 2021
Resumen La drepanocitosis, la enfermedad genetica mas frecuente en Francia, no solamente es una enfermedad de la hemoglobina, sino tambien una enfermedad vascular asociada a fenomenos inflamatorios. El dolor ocupa el primer plano. Se ha convertido en una enfermedad cronica salpicada de complicaciones agudas.
B Quinet
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Resumen La drepanocitosis, la enfermedad genetica mas frecuente en Francia, no solamente es una enfermedad de la hemoglobina, sino tambien una enfermedad vascular asociada a fenomenos inflamatorios. El dolor ocupa el primer plano. Se ha convertido en una enfermedad cronica salpicada de complicaciones agudas.
B Quinet
exaly +2 more sources
EMC Pediatria, 2006
La drepanocitosis o anemia de celulas falciformes es una enfermedad genetica de la hemoglobina que se transmite por herencia autosomica recesiva. La enfermedad se produce por una mutacion puntual del sexto codon del gen de la β-globina. La mutacion provoca la sintesis de una hemoglobina anormal, la hemoglobina S (HbS).
Robert Girot
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La drepanocitosis o anemia de celulas falciformes es una enfermedad genetica de la hemoglobina que se transmite por herencia autosomica recesiva. La enfermedad se produce por una mutacion puntual del sexto codon del gen de la β-globina. La mutacion provoca la sintesis de una hemoglobina anormal, la hemoglobina S (HbS).
Robert Girot
exaly +2 more sources
Síndrome hiperhemolítico en gestante con drepanocitosis: desenlace fatal
Progresos En Obstetricia Y Ginecologia, 2012Resumen La drepanocitosis es una enfermedad caracterizada por la presencia de una hemoglobina anomala. Afecta principalmente a la raza negra. Su diagnostico y su tratamiento en la gestante son de vital importancia, ya que puede tener repercusiones fatales tanto para la madre como para el feto.
María Guzmán Muñoz +6 more
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Descripción de un caso de drepanocitosis y consideraciones anestésicas
Revista Española De Anestesiología Y Reanimación, 2009Sickle cell anemia is the most common hemoglobinopathy. Advances in therapeutic techniques and anesthetic procedures have led to a considerable increase in the success of surgical procedures in these patients. We report the case of a 16-year-old black boy diagnosed with sickle cell anemia and beta-thalassemia who presented with chronic osteomyelitis of
L.A. Fernández-Meré +2 more
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Lesioni ossee simmetriche e drepanocitosi
Medico e Bambino Pagine elettroniche, 2023An 8-year-old boy suffering from sickle cell disease (SCD) was admitted to emergency unit complaining of moderate-to-severe pain in his lower limbs. He received chronic transfusion therapy and hydroxyurea. Apparently, he had never experienced vaso-occlusive crises (VOC) before.
Franzone, Daniele +5 more
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Il gioco delle parti: bronchiolite e drepanocitosi
Medico e Bambino Pagine elettroniche, 2023The case of a 2-month-old Senegalese infant with severe anaemia and RSV-related bronchiolitis is described. The Authors stress the role of common infections in leading to the diagnosis of sickle cell anaemia.
Izzo, Benito P.E. +4 more
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Risultati delle nostre osservazioni sulla Drepanocitosi e Thalassodrepanocitosi
Acta geneticae medicae et gemellologiae, 1959SUMMARYThe Authors studied 60 individuals bearing a positive test of sickle shaped cells (40 healthy bearers and 20 sick people).Drepanocytosis besides causing a Splenomegalic haemolitic disease in an homozygous state can also cause it in pure heterozygous individuals of high expressivity.
I. Gatto, G. Russo
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Drepanocitosi e osteonecrosi avascolare della testa del femore
Medico e Bambino Pagine elettronicheA 10.5-year-old girl with homozygous sickle cell disease on chronic treatment with hydroxyurea, blood transfusions and erythroexchange presented with sudden right thigh pain and limping, without trauma or fever. Imaging and lab results indicated avascular necrosis (AVN) of the femoral head.
Perfetto Francesca +6 more
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