Neurofibromatosis is a genetic disorder that causes tumors to grow along nerves in the body, skin, and brain. These tumors are usually noncancerous, but they can lead to skin changes, bone deformities, hearing or vision problems, and learning difficulties depending on their size and location. There are three main types - NF1, NF2, and schwannomatosis - each with different symptoms and severity. The condition is inherited in most cases, though it can also occur through random genetic mutation. |

CDKL5 deficiency disorder (CDD) is a genetic condition that causes seizures and significant delays in many aspects of development. CDD is about #MoreThanSeizures, it’s about daily challenges and interruptions to family life, it’s about skipping lunch to provide care. On World #CDKL5 Day, hear from Karen Utley, President & Co-Founder, International Foundation for CDKL5 Research, about her experiences. #CDKL5awareness | UCB Biopharma

A hormonal disorder causing enlarged ovaries with small cysts on the outer edges. The cause of polycystic ovary syndrome isn’t well understood, but may involve a combination of genetic and environmental factors. Symptoms include menstrual irregularity, excess hair growth, acne and obesity. Treatments such as birth control pills to regulate menstrual cycles, metformin to counter insulin resistance and prevent diabetes, statins to manage high cholesterol, hormones to boost fertility, and procedure