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Metabolic Geneticist

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Robyn M. Gillies

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Brisbane

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Services Offered by Robyn M. Gillies

  • Hyperthermia

  • Central Core Disease

  • Congenital Fiber-Type Disproportion

  • Cramp-Fasciculation Syndrome

  • High Potassium Level

  • Metabolic Acidosis

  • Osteolysis Syndrome Recessive

About Of Robyn M. Gillies

Robyn M. Gillies is a female healthcare provider who helps patients with various medical conditions like Hyperthermia, Central Core Disease, and High Potassium Level. She also specializes in treating conditions such as Congenital Fiber-Type Disproportion, Cramp-Fasciculation Syndrome, Metabolic Acidosis, and Osteolysis Syndrome Recessive.

Robyn M. Gillies uses her special skills and treatments to care for patients and make them feel better. She communicates with patients in a friendly and caring way, which helps them trust her and feel comfortable during their treatment.

To stay updated with the latest medical knowledge and research, Robyn M. Gillies regularly reads medical journals and attends conferences. This helps her provide the best possible care to her patients.

Robyn M. Gillies works closely with her colleagues and other medical professionals to ensure that patients receive comprehensive care. She values teamwork and collaboration to achieve the best outcomes for her patients.

Through her dedication and expertise, Robyn M. Gillies has positively impacted many patients' lives and health. Patients appreciate her compassionate approach and the personalized care she provides.

One of Robyn M. Gillies's notable publications is "Challenges and strategies for navigating Australian healthcare access: experience from Chinese international students." This publication reflects her commitment to improving healthcare access and equity for all patients.

In summary, Robyn M. Gillies is a compassionate and skilled healthcare provider who goes above and beyond to ensure the well-being of her patients. Through her expertise, communication skills, and commitment to staying updated with the latest research, she continues to make a positive impact on the lives of those she cares for.

Publications by Robyn M. Gillies

Frequently Asked Questions About Robyn M. Gillies

What conditions does Robyn M. Gillies specialize in as a Metabolic Geneticist?

Robyn M. Gillies specializes in diagnosing and managing inherited metabolic disorders such as phenylketonuria, maple syrup urine disease, and lysosomal storage disorders.

What diagnostic tests does Robyn M. Gillies perform to identify metabolic genetic disorders?

Robyn M. Gillies may conduct genetic testing, metabolic screening tests, enzyme assays, and molecular testing to diagnose metabolic genetic disorders in patients.

What treatment options does Robyn M. Gillies offer for patients with metabolic genetic disorders?

Robyn M. Gillies may recommend dietary modifications, enzyme replacement therapy, gene therapy, and other personalized treatment plans to manage metabolic genetic disorders effectively.

How can patients prepare for their initial consultation with Robyn M. Gillies?

Patients should bring their medical history, any previous test results, a list of current medications, and questions about their condition to discuss with Robyn M. Gillies during the consultation.

What ongoing support does Robyn M. Gillies provide to patients and their families dealing with metabolic genetic disorders?

Robyn M. Gillies offers genetic counseling, coordinates multidisciplinary care, provides education on managing the disorder, and supports families in navigating the challenges associated with metabolic genetic disorders.

What research or clinical trials is Robyn M. Gillies currently involved in related to metabolic genetic disorders?

Robyn M. Gillies may be actively involved in research studies or clinical trials aimed at advancing the understanding and treatment of metabolic genetic disorders, offering eligible patients opportunities to participate in cutting-edge research.
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