by Remember The Girls | May 6, 2022
Back to Previous NEMO Deficiency Syndrome The NEMO deficiency syndrome is a complex disease caused by genetic mutations in the X-linked NEMO gene (also known as IKK gamma or IKKG). It can involve many different parts of the body and often manifests in different ways...
by Remember The Girls | May 6, 2022
Back to Previous Nephrogenic Diabetes Insipidus (X-Linked) Nephrogenic diabetes insipidus is a rare hereditary disorder, most commonly transmitted in an X chromosome-linked recessive manner and characterized by the lack of renal response to the action of antidiuretic...
by Remember The Girls | May 5, 2022
Back to Previous Norrie Disease Norrie disease is characterized by vision loss at birth or a few weeks after an eye lesion such as retinal detachment occurs which threatens vision and can lead to severe visual impairment or loss of vision. Norrie disease mostly occurs...
