Learn how the complications of Neurofibromatosis Type 1 (NF1) are treated.
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) 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.
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.
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.
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.
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.
Read about the many different types of low-grade gliomas, including cerebellar, optic, brainstem, hemispheric, thalamic, and spinal cord.
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.
Learn about the different types of treatment for children with acute lymphoblastic leukemia (ALL).
Learn how children with acute myeloid leukemia (AML) are treated.
This section describes the treatment options for both acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML).
Teens learn about the two main approaches to hemophilia treatment: on-demand and prophylaxis.
Brain disorders can be caused by medical conditions, illness or injury. Find out how they can affect a child's mental health and overall functioning.
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.
Inhibitors are a type of immune complication that some people with hemophilia may develop. Learn more about inhibitors and how they are treated.
An in-depth look at treatment possibilities for other tumour types such as a pituitary adenoma, a schwannoma, a meningioma, and PNETs.
Does your child have autoimmune hepatitis? Learn the facts and how you can help.
In type 2 diabetes, the body does not produce enough insulin, or it cannot properly use what it produces. Learn how type 2 diabetes is managed.
Type 2 diabetes is less common in children and teens than in adults. Learn the signs of type 2 diabetes and how it is diagnosed.
Learn about laparoscopic surgery, a technique that uses small cuts to insert a camera and tools into the abdomen or pelvic area to perform a surgical procedure.
Learn about how acute myeloid leukemia (AML) develops and what factors may affect the development of the disease.
