Matthew I. Bellgard

Geneticist

MalešŸ“ Murdoch

About of Matthew I. Bellgard

Matthew I. Bellgard is a Geneticist based at South St, Murdoch, WA 6150, Australia. He works with people and families who are dealing with health issues that may have a genetic link. Genetic conditions can be confusing and stressful, especially when you’re trying to understand what’s going on and what it might mean for the future.


In many cases, Matthew helps people make sense of genetic testing results. This can be for children, teens, or adults. Sometimes people come in because there’s a strong family history. Other times it’s because symptoms are showing up but the cause isn’t clear yet. Over time, genetic clues can help guide next steps, including how to manage symptoms and what to watch for.


Matthew’s work includes conditions such as Angelman syndrome and other movement or developmental disorders. He also looks at muscle-related genetic conditions like Duchenne muscular dystrophy and Becker muscular dystrophy. High cholesterol and cholesterol-related genetic conditions are another key focus, including familial hypercholesterolaemia and homozygous familial hypercholesterolaemia (HoFH). He also supports people with lysosomal and metabolic conditions, including Gaucher disease and lysosomal acid lipase deficiency.


Sometimes the presenting issue is unusual, like hyperhidrosis (sweating issues), ganglion cysts, or tick paralysis. In these situations, genetic input can help when it’s needed, or it can help confirm that another cause is more likely. Geneticists don’t just focus on one thing. They think about the pattern of symptoms, family history, and test results together.


Matthew’s training is grounded in medical genetics. That means he’s set up to explain results in plain language and to talk through what the findings could mean, without the heavy medical jargon. He aims for a calm, practical approach, because people often have lots of questions and they may feel overwhelmed.


Genetic medicine keeps moving, and new findings can change how doctors think about certain conditions. Matthew stays across current genetic research where it matters for day-to-day care. At times, the team may also discuss clinical trial options if a trial is relevant and available, especially when a condition has limited treatment choices.


If you’re looking for help understanding a possible genetic cause, or you want to talk through genetic testing and next steps in Murdoch, Matthew I. Bellgard is located on South St in Murdoch, WA 6150.

Services & Conditions Treated

Angelman SyndromeTick ParalysisBecker Muscular DystrophyDefective Apolipoprotein B-100Duchenne Muscular DystrophyFamilial HypercholesterolemiaGanglion CystGaucher DiseaseHigh CholesterolHomozygous Familial Hypercholesterolemia (HoFH)HyperhidrosisLysosomal Acid Lipase DeficiencyMovement Disorders

Publications

1 total

Association Between Challenging Behaviour and Sleep Problems in Adults Enrolled in the Global Angelman Syndrome Registry.

Journal of autism and developmental disorders • April 19, 2024

Frequently Asked Questions

What services does Dr Matthew Bellgard offer?
Dr Bellgard provides genetic consultation and testing related to conditions such as Angelman Syndrome, Becker Muscular Dystrophy, Duchenne Muscular Dystrophy, Familial Hypercholesterolemia (including HoFH), Gaucher Disease and other genetic conditions. He also works with related disorders like movement disorders and lipid-related conditions.
Which conditions does he treat?
He focuses on genetic and metabolic conditions including Angelman Syndrome, Duchenne and Becker muscular dystrophies, hypercholesterolaemia and familial hypercholesterolemia, lysosomal storage disorders, Gaucher Disease, and related movement disorders.
Where is his practice located?
His services are available at a clinic on South Street in Murdoch, WA 6150, Australia.
How can I book an appointment?
To book an appointment, contact the clinic or practice where Dr Bellgard works. They can provide available times and guidance on the referral or assessment process.
Does he treat high cholesterol or familial hypercholesterolemia?
Yes. He covers conditions like high cholesterol and familial hypercholesterolemia, including homozygous familial hypercholesterolemia (HoFH).
What should I expect in a genetic consultation?
A genetic consultation typically involves reviewing medical and family history, discussing potential genetic tests, and explaining what results might mean for you or your family. Specific steps will be guided by your individual case and needs.

Contact Information

South St, Murdoch, WA 6150, Australia

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