Discover the main features and causes of attention deficit hyperactivity disorder, which affects one in 20 children.
Down syndrome is a genetic condition present at birth. Learn about the symptoms, complications and outlook for children with Down syndrome.
Discover the main signs and symptoms of ADHD in school-aged children and teens.
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 to support a child with epilepsy who experiences some of the cognitive consequences associated with the condition.
Learn about CYP2D6, a gene tested through pharmacogenetic testing to predict an individual’s response to certain medications.
Find out how structure, consistency and clear communication can help you support a child with ADHD symptoms.
Genetic counselling is a process that provides information and support to individuals and families at risk of, or with, a genetic condition.
Myotonic dystrophy type 1 (DM1) disease is a genetic disorder that causes muscle stiffness, that over time causes the muscles to become weaker and smaller.
Skeletal dysplasia is a term used to describe a group of genetic conditions that cause abnormal formation of bone and cartilage. Growth and other bodily functions may also be affected.
Learn about attention deficit hyperactivity disorder (ADHD) and what you can do to help your child at home and at school.
This page explains the diagnosis and treatment of primary immune deficiency (PID), a genetic condition that weakens the immune system.
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.
Charcot-Marie-Tooth (CMT) is a genetic disease that affects the nerves that connect the spinal cord to the muscles and sensory receptors in the body, leading to muscle wasting, loss of sensation and challenges with balance and coordination.
Information for parents about infantile osteopetrosis, a rare genetic condition that may cause fractures, short stature (height), recurrent infections, hearing loss and vision problems.
Find out how medications can work with behavioural treatment to help a child with ADHD symptoms.
Find out how to work with your child's school to support your child with ADHD.
Read about the causes, symptoms and treatments for generalized epilepsy syndromes.
22q11DS is a genetic condition with a wide range of symptoms. Learn about some of the more common medical features of 22q11DS.
Children with Down syndrome may be at a higher risk for some medical conditions. Learn what these conditions are and how to manage them.
Spinal muscular atrophy (SMA) is a genetic disorder that causes muscle weakness and muscle atrophy (shrinking), and can affect a child’s ability to speak, walk, and breathe.
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.
Understanding your child's cleft lip and/or palate through genetic assessments.
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.
Congenital myasthenic syndrome (CMS) is caused by genetic mutations that cause problems with nerve-to-muscle communication leading to muscle weakness and fatigue.
