by Remember The Girls | Jul 1, 2022
Back to Previous Hemophilia A/B Hemophilia is usually an inherited bleeding disorder in which the blood does not clot properly. This can lead to spontaneous bleeding as well as bleeding following injuries or surgery. Blood contains many proteins called clotting...
by Remember The Girls | Jul 1, 2022
Back to Previous Hunter Syndrome (Mucopolysaccharidosis Type II) Mucopolysaccharidosis type II (MPS II) is a rare lysosomal inborn error of metabolism that affects every organ of the body. Although the age of onset, disease severity and the rate of progression of the...
by Remember The Girls | Jul 1, 2022
Back to Previous Hyper IgM Syndromes Hyper IgM syndromes are a group of rare disorders in which the immune system does not function properly. They are classified as rare primary immunodeficiency disorders, which are a group of disorders characterized by irregularities...
by Remember The Girls | Jul 1, 2022
Back to Previous HNRNPH2-Related Neurodevelopmental Disorder Most individuals with HNRNPH2-related neurodevelopmental disorder (HNRNPH2-NDD) have symptoms early in life, before age 12 months. The major features of HNRNPH2-NDD are developmental delay / intellectual...
by Remember The Girls | Jul 1, 2022
Back to Previous Hypophosphatemia (X-Linked) X-linked hypophosphatemia (XLH) is an inherited disorder characterized by low levels of phosphate in the blood. Phosphate levels are low because phosphate is abnormally processed in the kidneys, which causes a loss of...
