A list of websites with in-depth information on neurofibromatosis type 1 (NF1) in children.
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.
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.
Learn how the complications of Neurofibromatosis Type 1 (NF1) are treated.
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.
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 different brain tumors including pituitary adenoma, schwannoma, meningioma, and PNETs. Trusted answers from The Hospital for Sick 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.
An in-depth look at treatment possibilities for other tumour types such as a pituitary adenoma, a schwannoma, a meningioma, and PNETs.
Learn about how acute myeloid leukemia (AML) develops and what factors may affect the development of the disease.
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.
An overview of the causes, genetics, symptoms, diagnosis, environmental risks and treatment of childhood brain tumours.
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.
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.
In type 1 diabetes, the pancreas stops producing insulin. Learn the symptoms, causes and how this life-long condition is diagnosed.
This page lists the different types of arthritis that can arise in young people. Knowing the type of arthritis you have can help you understand your condition and how it will do over time.
Your child needs to be given a vaccine called haemophilus influenzae type B vaccine. This information sheet explains what haemophilus influenzae type B vaccine does, how it is given, and what side effects or problems your child may have when they take this medicine.
Von Willebrand disease is a condition that affects the blood’s ability to clot properly. Learn about the different types of this disease and how they are treated.
Find out about the two most common types of diabetes: type 1 and type 2 diabetes. Symptoms and causes differ for each.
Oligoarticular arthritis is the most common type of arthritis in young people, affecting four joints or less in the first six months of symptoms. Find out more about the two different types of oligoarticular arthritis.
