Sickle cell trait (SCT), a commonly asymptomatic condition, has many associated clinical
complications that upon presentation, can be very difficult to attribute to SCT. The effects of …

Sickle cell trait (SCT), the heterozygous state of the sickle hemoglobin beta globin gene
(HbAS) is carried by as many as 100 million individuals including up to 25% of the …

Background Patients with sickle cell trait (SCT) generally suffer few effects of sickle cell
disease. Acute splenic syndrome is a rare but well-documented complication of SCT that …

TORREGROSA, José V. et al. Tratamiento eficaz de la arteriolopatía urémica calcificante
con bifosfonatos. Nefrología (Madr.)[online]. 2012, vol. 32, n. 3, pp. 329-334. ISSN 0211 …

We report a case of splenic infarction in a patient with sickle cell traits (SCT), focusing on the
computed tomography (CT) findings. The patient was an African-American man in his …

Sickle‐cell trait is a common genetic abnormality in the African American population. A
sickle‐cell crisis in a patient with sickle‐cell trait is uncommon at best. Abdominal painful …

Acute splenic infarction in otherwise asymptomatic individuals harbouring sickle cell trait
(SCT) may occur when they are exposed to low oxygen tension at high altitudes. 1 The first …

Generalmente, los pacientes con rasgo falciforme sufren pocas manifestaciones del
espectro de la anemia de células falciformes. El infarto esplénico es raro, pero es una …

Splenic infarction might be the symptom onset of an important underlying disease. The
possibility of splenic infarction must be inserted into differential diagnosis in all those …

La Anemia drepanocítica es una enfermedad genética con patrón de herencia autosómico
recesivo, caracterizada por la presencia de eritrocitos en forma de hoz, los cuales no …