Neurofibromatosis Type 1 (NF1) occurs because of a mutation to the NF1 gene. About half of cases are spontaneous mutations, while the other half are inherited from a parent to a child.
A list of websites with in-depth information on neurofibromatosis type 1 (NF1) in children.
Genetic counselling helps people understand genetic or inherited disorders. It can help families learn about neurofibromatosis type 1 (NF1) and decide if testing is right for them.
Neurofibromatosis type 1 (NF1) is a skin condition that causes growths on nerves. Find out what NF1 genetic testing is, what the test results mean and why to consider testing for it.
Learn about clinical and genetic testing, two ways that doctors diagnose Neurofibromatosis Type 1 (NF1). Each of these methods has advantages and limits.
Learn how the complications of Neurofibromatosis Type 1 (NF1) are treated.
Neurofibromatosis or NF1 causes growths to form on nerve tissues. Learn about both the common and uncommon skin and bone abnormalities of this condition.
A child with neurofibromatosis type 1 must have consistent medical care. Parents can use this checklist to ensure their child receives all the care they need.
Genetics can play an important role in your family's health. Learn more about genetics; genetic counselling, screening, and diagnosis; different genetic conditions; and how genetics relate to understanding and managing overall health.
Plexiform neurofibromas (PNs) are types of tumours that grow along nerves, most commonly occurring in children with neurofibromatosis type 1 (NF1). Learn about the symptoms, causes, treatment and long-term outcomes.
Acute lymphoblastic leukemia (ALL) is the most common childhood cancer. Learn about how this cancer develops and what factors may affect the development of the disease.
Read about the many different types of low-grade gliomas, including cerebellar, optic, brainstem, hemispheric, thalamic, and spinal cord.
Find out how genetics play a part in many types of epilepsy.
An overview of the causes, genetics, symptoms, diagnosis, environmental risks and treatment of childhood brain tumours.
Learn about genetics and how genetics contribute to health and disease.
Discover why you or your child may have been referred for a genetics appointment and what to expect when you see a geneticist and/or a genetic counsellor.
Learn about genetics in the context of pharmacogenetics (PGx) and precision medicine.
Albinism is a genetic condition that causes a person to have no, or very little, pigment in the eyes and sometimes in the skin and hair also. Albinism is passed from parent to child because of a genetic mutation.
In type 1 diabetes, the pancreas stops producing insulin. Learn the symptoms, causes and how this life-long condition is diagnosed.
An in-depth look at treatment possibilities for other tumour types such as a pituitary adenoma, a schwannoma, a meningioma, and PNETs.
Hereditary spherocytosis is a genetic condition. In most cases it is inherited from a parent. Learn how HS is inherited and what happens in a de novo mutation.
Learn about how acute myeloid leukemia (AML) develops and what factors may affect the development of the disease.
Learn about the role that genetics plays in many heart conditions that afflict children.
Café-au-lait macules are flat marks on the skin. Find out how CALMs are diagnosed, how they affect the body and how they are treated.
