Lymphatic malformations (LMs) are rare, congenital anomalies of the lymphatic system, which is part of the circulatory system and crucial...
Rare disease
Epidermolysis Bullosa (EB) is a group of rare genetic disorders characterized by fragile skin that blisters and tears from minor...
Duchenne Muscular Dystrophy (DMD) is the most common form of muscular dystrophy characterised by progressive skeletal muscle degeneration and weakness....
Spinal Muscular Atrophy (SMA) is a genetic neurodegenerative disease that leads to progressive muscle weakness and paralysis and if left...
Alagille syndrome (ALGS) is a rare genetic disorder that affects around one in every 30,000 live births. It results from...
Myasthenia gravis (MG) is a rare neuromuscular disorder that affects the transmission of signals between nerves and muscles. It is...
Pompe disease, also known as glycogen storage disease type II, is a rare genetic disorder that affects approximately 1 in...
What is Sarcoidosis? Sarcoidosis is a rare disease where inflamed cells clump together to make small lumps called granulomas which...
Calciphylaxis is an uncommon, rare, serious, and fatal disorder that is characterized by: Calcification of the small blood vessels...
Anaplastic large-cell lymphoma (ALCL) is a rare type of non-Hodgkin lymphoma that T-cells. Pathologically, T-cells appear abnormal, large, and undeveloped. Most patients are...
