Lymphatic malformations (LMs) are rare, congenital anomalies of the lymphatic system, which is part of the circulatory system and crucial...
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...
In 2018, the estimated incidence of prostate cancer was high, with Japan accounting for 6% (78,400 people) of the total...
The global pandemic, COVID-19, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is ongoing. Although numerous effective vaccines have...
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...
INTRODUCTION Dr. Ahmed Farrag is a hematology and internal medicine specialist at the Thalassemia Centre at Latifa Women and Children...
