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.
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.
Cleidocranial dysplasia is a genetic disorder that affects the development of bones and teeth. Learn what to expect with a diagnosis of CCD.
Information for parents about hereditary multiple osteochondromas (previously called hereditary multiple exostoses), a genetic condition that causes growths (bumps) on the bones.
Information for parents about trisomy 13, a rare genetic condition that causes developmental delay and affects many different organ systems.
Noonan syndrome is a genetic condition. Learn about the symptoms and diagnosis of Noonan syndrome and the heart conditions associated with the condition.
Information about campomelic dysplasia, a genetic condition that affects the development of the skeleton and reproductive system.
Information for parents about trisomy 18, a rare genetic condition that causes developmental delay and affects many different organ systems.
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.
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 the genetic neuromuscular disorder called Friedreich ataxia (FRDA).
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.
Information for parents about infantile osteopetrosis, a rare genetic condition that may cause fractures, short stature (height), recurrent infections, hearing loss and vision problems.
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 the genetic causes of 22q11 deletion syndrome, risk factors and confirming diagnosis.
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.
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.
Learn about clinical and genetic testing, two ways that doctors diagnose Neurofibromatosis Type 1 (NF1). Each of these methods has advantages and limits.
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.
22q11 deletion syndrome (22q11DS) is a genetic condition. Learn what causes it, how it's diagnosed and treated.
