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Metabolic Geneticist

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Katherine E. Lewis

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Westmead

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Services Offered by Katherine E. Lewis

  • 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency

  • Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease)

  • Mongolian Blue Spots

  • Primary Lateral Sclerosis

  • Carnitine-Acylcarnitine Translocase Deficiency

  • Gangliosidosis

  • GM1 Gangliosidosis

  • Metabolic Acidosis

  • Phenylketonuria (PKU)

About Of Katherine E. Lewis

Katherine E. Lewis is a female healthcare provider who helps people with different health conditions like 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Amyotrophic Lateral Sclerosis (ALS), Mongolian Blue Spots, and more. She has special skills to treat these conditions.

Katherine E. Lewis talks to her patients in a friendly way, making them feel comfortable and cared for. Patients trust her because she listens to their concerns and explains things clearly.

To stay updated with the latest medical knowledge, Katherine E. Lewis reads scientific articles and attends conferences. She also works with other healthcare professionals to learn new things and improve patient care.

Katherine E. Lewis works well with her colleagues, sharing knowledge and supporting each other. This teamwork helps them provide the best care for their patients.

Katherine E. Lewis has made a positive impact on patients' lives by improving their quality of life and healthcare services. Her research on caregiver quality of life and healthcare for children with dementia has been published in a medical journal.

She is also involved in a clinical trial for Phenylketonuria treatment, showing her dedication to finding better ways to help patients with this condition.

In summary, Katherine E. Lewis is a caring and skilled healthcare provider who works hard to improve the lives of her patients. Through her research and clinical trials, she aims to make a positive difference in the healthcare field.

Publications by Katherine E. Lewis

Clinical Trials by Katherine E. Lewis

A Phase 3 Open-Label Study of PTC923 (Sepiapterin) in Phenylketonuria

Enrollment Status: Recruiting

Published: March 20, 2025

Intervention Type: Drug

Study Drug: PTC923

Study Phase: Phase 3

Frequently Asked Questions About Katherine E. Lewis

What is a Metabolic Geneticist and what conditions do they specialize in?

A Metabolic Geneticist like Katherine E. Lewis specializes in inherited metabolic disorders, which are conditions caused by defects in enzymes that help the body metabolize substances.

What services does Katherine E. Lewis offer?

Katherine E. Lewis offers comprehensive genetic testing, personalized treatment plans, and ongoing management for individuals with metabolic disorders.

How can I schedule an appointment with Katherine E. Lewis?

To schedule an appointment with Katherine E. Lewis, you can contact her office directly or ask for a referral from your primary care physician.

What should I expect during a consultation with Katherine E. Lewis?

During a consultation with Katherine E. Lewis, she will review your medical history, perform a physical examination, and discuss genetic testing options and treatment plans tailored to your specific needs.

What are some common symptoms of metabolic disorders that Katherine E. Lewis can help with?

Common symptoms of metabolic disorders include developmental delays, failure to thrive, seizures, metabolic crises, and abnormal laboratory test results, all of which Katherine E. Lewis can assist in diagnosing and managing.

How can Katherine E. Lewis help me manage my metabolic disorder on a day-to-day basis?

Katherine E. Lewis can provide guidance on dietary modifications, medication management, monitoring for potential complications, and coordinating care with other specialists to help you effectively manage your metabolic disorder.

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