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.
Learn about clinical and genetic testing, two ways that doctors diagnose Neurofibromatosis Type 1 (NF1). Each of these methods has advantages and limits.
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 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.
Read about the many different types of low-grade gliomas, including cerebellar, optic, brainstem, hemispheric, thalamic, and spinal cord.
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.
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.
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.
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.
An in-depth look at treatment possibilities for other tumour types such as a pituitary adenoma, a schwannoma, a meningioma, and PNETs.
Learn about different brain tumors including pituitary adenoma, schwannoma, meningioma, and PNETs. Trusted answers from The Hospital for Sick Children.
In type 1 diabetes, the pancreas stops producing insulin. Learn the symptoms, causes and how this life-long condition is diagnosed.
An overview of the causes, genetics, symptoms, diagnosis, environmental risks and treatment of childhood brain tumours.
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.
Complete this module to learn all about cross-contamination and how to read ingredient labels to help you follow the gluten-free diet.
Celiac disease is a lifelong condition. These eLearning modules will help you learn about the symptoms of celiac disease, how celiac disease is diagnosed, how it is treated and how gluten affects people with celiac disease. Also learn about special considerations for people who have both celiac disease and type 1 diabetes.
There are many types of cancer that can be diagnosed in children and teenagers. Learn about where to find information on different cancers and the types of questions you can ask your health-care team.
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.
Acute myeloid leukemia is a type of leukemia. Find out how AML starts, diagnosis and possible symptoms.
Germ cell tumours are a type of cancer that start in the germ cells. Learn about where germ cell tumours are most commonly found, how they are diagnosed and the main types of treatment.
