Hemoglobin
SC disease, is a type of sickle cell disease, which means it affects the shape of the red blood cells.
This is a unique case of massive ovarian edema caused by a vasoocclusive crisis in a girl with hemoglobin
SC disease.
Hemoglobin
SC disease and hemoglobin S[[beta].sup.+] thalassemia are other common forms of SCD.
Functional asplenia in hemoglobin
SC disease. Blood 1995 Apr; 85(8):2238-2244.
Sickle cell anemia (HbSS/HbS-Beta thalassemia zero) accounts for 70% of cases of sickle cell disease in populations of African ethnicity, with most of the remainder having hemoglobin
SC disease (HBSC disease) due to the coinheritance of the [[beta].sup.s] and [[beta].sup.c] alleles [2,3].
Mobile Right Atrial Thrombi in a Patient with the Hemoglobin
SC Disease. Case Rep Med.
There have been case reports of luteal cyst rupture with massive hemoperitoneum during dialysis, thrombolytic therapy, patient with Hb
SC disease, liver disease and patient on anticoagulation therapy.
The above cases represent four different scenarios of
SC disease in children with malignancies.
Some people with this genotype develop Hb
SC disease, a variant of sickle cell disease.
We encountered a 62-year-old man with hemoglobin (Hb)
SC disease. Diabetes mellitus had been previously diagnosed in this patient on the basis of 2 increased fasting glucose values.
Hydroxyurea therapy for pediatric patients with hemoglobin
SC Disease. Journal of Pediatric Hematology/Oncology, 23(5), 306-308.
'Haemoglobin
SC disease' and 'sickle beta thalassaemia' are similar conditions.