Peter D. Currie

Neuromuscular Specialist

Male📍 Clayton

About of Peter D. Currie

Peter D. Currie is a neuromuscular specialist based in Wellington Road, Clayton, VIC 3800, Australia. He works with people who have muscle and nerve conditions that can affect strength, movement, and day to day life. This kind of care is often needed across childhood and into adulthood, and it can come with a lot of questions for families.


Peter focuses on neuromuscular disorders such as muscular dystrophies and myopathies. These can be present from birth or show up later. In many cases, symptoms build slowly, so getting the right diagnosis and support early can make a big difference. He also looks after people dealing with muscle wasting and related muscle problems.


Some of the conditions he sees include Duchenne muscular dystrophy and Becker muscular dystrophy, as well as limb-girdle muscular dystrophy and other inherited muscle disorders. He also works with people who have congenital muscular dystrophy type 1A, benign autosomal dominant myopathy, collagen VI–related myopathy, and nemaline myopathy. There are also rarer forms of myopathy listed under his care, including tubular aggregate myopathy and x-linked myotubular myopathy.


Over time, neuromuscular conditions can affect more than just muscles. They can change how someone moves, how they use their arms and legs, and how they manage fatigue. At times, other parts of health can be involved too, so it helps when care is calm, clear, and practical. Peter’s approach is focused on understanding what is going on and supporting ongoing management as needs change.


Peter’s professional work includes publications, although the specific titles and details are not shown here. If research is relevant to a patient’s situation, it can help guide the kind of care and follow up that is considered. Clinical trial information isn’t listed here, so trial options would need to be discussed directly during an appointment if they come up.


As for education and work history, these details are not provided in the information shown here. What matters most is that Peter provides neuromuscular specialist care in the Clayton area and helps patients and families deal with inherited muscle conditions in a steady, down-to-earth way.

Services & Conditions Treated

Congenital Muscular Dystrophy Type 1ABecker Muscular DystrophyBenign Autosomal Dominant MyopathyCollagen VI-Related MyopathyCongenital Fiber-Type DisproportionDuchenne Muscular DystrophyFrontonasal Dysplasia Klippel Feil SyndromeKlippel-Feil SyndromeLimb-Girdle Muscular DystrophyLimb-Girdle Muscular Dystrophy Type 2IMuscle AtrophyNemaline MyopathyTubular Aggregate MyopathyX-Linked Myotubular Myopathy

Publications

1 total

Generation of an iPSC line (with isogenic control) from the PBMCs of a COL6A1 (c.1056 + 2T > A) Bethlem myopathy patient.

Stem cell research • January 17, 2024

Frequently Asked Questions

What services does Dr Peter D. Currie offer?
Dr Currie is a neuromuscular specialist with a focus on muscular dystrophy and related muscle disorders. He treats conditions such as Duchenne and Becker muscular dystrophy, various limb-girdle muscular dystrophies, congenital myopathies, and other muscle conditions listed in his service area.
Which conditions can I discuss with Dr Currie?
Conditions include Congenital Muscular Dystrophy Type 1A, Becker Muscular Dystrophy, Duchenne Muscular Dystrophy, Limb-Girdle Muscular Dystrophy, Nemaline Myopathy, Tubular Aggregate Myopathy, Klippel-Feil Syndrome and other listed myopathies. If you’re unsure, bring any symptoms or previous tests to help review.
Where is Dr Currie’s clinic located?
The clinic is on Wellington Road in Clayton, VIC 3800, Australia.
How do I book an appointment?
To book, contact the clinic where Dr Currie practices. The exact booking method (phone, online form, or in person) will be provided by the clinic. Have any previous test results handy to speed up the process.
What should I bring to my first visit?
Bring any relevant medical records, recent test results, and a list of current symptoms and medications. If you have family history of neuromuscular disorders, note that down as well.
What can I expect during a neuromuscular assessment?
Expect a review of your symptoms, a physical examination, and discussion of possible tests or referrals. The goal is to understand the condition and plan appropriate care or management.