What is Amyloidosis? An amyloidosis is a group of serious and rare diseases in which abnormal proteins, known as amyloid...
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Calciphylaxis is an uncommon, rare, serious, and fatal disorder that is characterized by: Calcification of the small blood vessels...
Char syndrome is a rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by: Triad of patent ductus arteriosus (PDA) Typical facial...
In December 2020, five (5) molecules were approved for the treatment of hematology/oncology disorders. Osimertinib for adjuvant therapy after tumor...
Sickle cell disease is a hereditary problem that causes a type of faulty hemoglobin in red blood cells. Hemoglobin carries...
It seems that the hope of gene therapy for transfusion-dependent β-thalassemia (TDT) is becoming so close. During the 62nd American Society...
In November, three (3) indications/molecules were approved by FDA: Sonalleve MR-HIFU system for the treatment of osteoid osteoma in the...
Carcinoid syndrome usually takes place in patients with an advanced stage of carcinoid tumors. Carcinoid tumor is a type of rare...
Beta thalassemias is an inherited blood disorder that results from the reduced or absent synthesis of the beta chains of hemoglobin....
What is B-cell lymphoma? B-cell lymphomas are a type of blood cancer that developed more frequently in immunocompromised patients and...
