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گزارش یک مورد فنوتیپ نادر Rh--D: یک گزارش مورد

Background and Objective: Of all blood group systems, RH is one of the most important blood groups, which its compatibility is one of the essential principals of transfusion. Two genes (RhD and RhCE) locate on chromosome 1, and encode the Rh proteins. RhD is an immunogenic antigen. We describe a rare Rh phenotype D-- in this report. Case Report: A forty- nine- year- old man, who receiv...

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Leptospirosis is a Zoonotic disease that rarely manifests in a severe manner, (Weil's syndrome). Regarding epidemiology of this disease, in some rural areas of Mazandaran Province we encountered a rare case of acute pancreatitis during progression of severe Leptosprosis is presented herein. Patient is a 50 year old male farmer who was admitted to the hospital due to experiencing 10 days of fe...

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Heapatoblastoma is the most common primary malignant liver disease. It occures primarily in children younger than 3 years old. It is very rare in neonatal period. Most children present with an enlarging, asymptomatic abdominal mass. Serum alpha fetoprotein is elevated in 66 percent of patients, significant thrombocytosis, mild anemia and moderate leukocytosis are also common. Abdominal X-Rays d...

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Osteopetrosis is a rare metabolic bone disease characterized by generalized increase in skeletal mass. About 500 cases have been described in the literature. This disorder presents. In one of three forms: Osteopetosis Tarda , Osreopetrosis Congenital and “marble bone” disease. Osteopetrosis congentia results in bone marrow failur and is almost always fatal. Marble bone disease causes short st...