Nalamaree

Myositis

Myositis refers to inflammation of the muscles that you use to move your body. It’s a condition where your immune system mistakenly attacks your muscles, leading to chronic inflammation and muscle weakness.

Muscular Dystrophy

Muscular dystrophy (MD) refers to a group of genetic diseases that cause progressive weakness and degeneration of skeletal muscles.

Cystic Fibrosis

Cystic fibrosis is a chronic condition that requires lifelong management, including medications to thin mucus, antibiotics to treat infections, and therapies to help clear mucus from the lungs.

Haemophilia

Haemophilia (hemophilia), is a rare genetic blood disorder that affects the body’s ability to form blood clots. This can result in prolonged bleeding after an injury, as well as spontaneous bleeding.

Thalassemia & sickle cell anaemia

Thalassemia and sickle cell anemia are both genetic blood disorders that affect the structure and function of red blood cells, leading to various health complications.

Congenital megacolon or Hirschsprung's disease

Hirschsprung's disease, also known as congenital megacolon, is a rare condition characterized by the absence of nerve cells in the muscles of the colon (large intestine).

Pompe disease

Pompe disease, also known as glycogen storage disease type II or acid maltase deficiency, is a rare genetic disorder characterized by the buildup of glycogen in certain tissues and organs, particularly muscles.

Gaucher’s disease

Gaucher disease is a rare genetic disorder characterized by the deficiency of an enzyme called Glucocerebrosidase, which leads to the accumulation of a fatty substance called Glucocerebroside.

Disease