Genetic counselling is a process that provides information and support to individuals and families at risk of, or with, a genetic condition.
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.
Understanding your child's cleft lip and/or palate through genetic assessments.
Information for parents about hereditary multiple osteochondromas (previously called hereditary multiple exostoses), a genetic condition that causes growths (bumps) on the bones.
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.
Information for parents about trisomy 13, a rare genetic condition that causes developmental delay and affects many different organ systems.
Information for parents about trisomy 18, a rare genetic condition that causes developmental delay and affects many different organ systems.
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.
Noonan syndrome is a genetic condition. Learn about the symptoms and diagnosis of Noonan syndrome and the heart conditions associated with the 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.
Information about campomelic dysplasia, a genetic condition that affects the development of the skeleton and reproductive system.
Learn about the genetic neuromuscular disorder called Friedreich ataxia (FRDA).
Information for parents about infantile osteopetrosis, a rare genetic condition that may cause fractures, short stature (height), recurrent infections, hearing loss and vision problems.
Cleidocranial dysplasia is a genetic disorder that affects the development of bones and teeth. Learn what to expect with a diagnosis of CCD.
Information about cartilage-hair hypoplasia, a genetic condition that may cause short stature (height), shorter arms and legs than expected, fine, sparse hair and problems with blood and the immune system.
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 the supports available to families coping with pregnancy and infant loss, including perinatal palliative care.
Learn about clinical and genetic testing, two ways that doctors diagnose Neurofibromatosis Type 1 (NF1). Each of these methods has advantages and limits.
Learn about the genetic causes of 22q11 deletion syndrome, risk factors and confirming diagnosis.
If you are sexually active, there is a risk that you could get pregnant or get your partner pregnant. This page provides answers to some common questions you may have about pregnancy.
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.
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.
Primary ciliary dyskinesia (PCD) is a rare inherited disease that can cause recurring lung, ear and sinus infections. Find out how the condition is caused and treated and the long-term outlook for children with PCD.
22q11 deletion syndrome (22q11DS) is a genetic condition. Learn what causes it, how it's diagnosed and treated.
