Understanding Pompe Disease: Symptoms, Diagnosis, and Treatment
Pompe disease, also known as glycogen storage disease type II, is a rare genetic disorder that affects approximately 1 in...Read More
Gene therapy & β-thalassemia
It seems that the hope of gene therapy for transfusion-dependent β-thalassemia (TDT) is becoming so close. During the 62nd American Society of Hematology...Read More
What is Cushing syndrome?
Cushing syndrome is a rare benign or non-cancerous tumor. This syndrome affects both men and women, but it has a...Read More
Chronic diarrhoea or Carcinoid Syndrom
Carcinoid syndrome usually takes place in patients with an advanced stage of carcinoid tumors. Carcinoid tumor is a type of...Read More
What is Char syndrome?
Char syndrome is a rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by: Triad of patent ductus arteriosus (PDA)Typical facial features...Read More
What is Calciphylaxis?
Calciphylaxis is an uncommon, rare, serious, and fatal disorder that is characterized by: Calcification of the small blood vessels located...Read More
What is Amyloidosis?
What is Amyloidosis? An amyloidosis is a group of serious and rare diseases in which abnormal proteins, known as amyloid...Read More
What is Sarcoidosis?
Sarcoidosis is a rare disease where inflamed cells clump together to make small lumps called granulomas which can develop in...Read More
What is Wilson’s disease?
What is Wilson’s disease? Wilson’s disease is a rare genetic autosomal disease. It occurs in approximately one in 30,000 to...Read More
What is Alport syndrome?
Welcome to WordPress. This is your first post. Edit or del What is Alport syndrome? Alport syndrome is one of...Read More