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Geneticist

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Helen M. Mcrae

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Parkville

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Services Offered by Helen M. Mcrae

  • Borjeson-Forssman-Lehmann Syndrome

  • Calcinosis

  • Epilepsy

  • Hypogonadism

  • Hypogonadotropic Hypogonadism

  • Isolated Hypogonadotropic Hypogonadism

  • Obesity

About Of Helen M. Mcrae

Helen M. Mcrae is a female medical professional who helps people with different health problems like Borjeson-Forssman-Lehmann Syndrome, Calcinosis, Epilepsy, Hypogonadism, Hypogonadotropic Hypogonadism, Isolated Hypogonadotropic Hypogonadism, and Obesity.

Helen M. Mcrae uses special skills and treatments to care for patients. She talks to patients in a kind and clear way, making them feel comfortable and safe. Patients trust her because she listens to their concerns and explains things in a simple manner.

To help patients better, Helen M. Mcrae keeps learning about new medical information and research. She reads medical journals and attends conferences to stay updated. This helps her give the best care to her patients.

Helen M. Mcrae works well with other medical professionals. She shares knowledge and collaborates with colleagues to provide the best treatment for patients. This teamwork approach helps patients get the care they need.

Helen M. Mcrae's work has had a positive impact on many patients' lives. For example, her research on the Börjeson-Forssman-Lehmann intellectual disability syndrome has helped understand the condition better. Her dedication to improving patient care shows in the positive outcomes she achieves.

One of Helen M. Mcrae's notable publications is "Loss of PHF6 causes spontaneous seizures, enlarged brain ventricles and altered transcription in the cortex of a mouse model of the Börjeson-Forssman-Lehmann intellectual disability syndrome." This study, published in PLoS genetics, sheds light on the syndrome and how it affects the brain.

In summary, Helen M. Mcrae is a caring and knowledgeable medical professional who uses her skills to help patients with various health conditions. She stays updated with the latest medical knowledge, works well with colleagues, and has made a positive impact on patients' lives through her research and patient care.

Publications by Helen M. Mcrae

Frequently Asked Questions About Helen M. Mcrae

What conditions or diseases does Helen M. Mcrae specialize in as a Geneticist?

Helen M. Mcrae specializes in diagnosing and treating a wide range of genetic conditions and diseases, including but not limited to inherited disorders, chromosomal abnormalities, and genetic predispositions to certain diseases.

What services does Helen M. Mcrae offer to patients seeking genetic counseling?

Helen M. Mcrae offers genetic counseling services to individuals and families, which may include genetic testing, risk assessment, family history evaluation, and personalized management plans based on genetic findings.

How can Helen M. Mcrae help patients understand their genetic test results?

Helen M. Mcrae provides comprehensive explanations of genetic test results to patients, helping them interpret the findings, understand the implications for their health, and make informed decisions about their care and future health management.

What are some common reasons patients seek consultations with Helen M. Mcrae?

Patients often seek consultations with Helen M. Mcrae for reasons such as family history of genetic disorders, concerns about inherited conditions, prenatal genetic testing, carrier screening, or genetic risk assessment for certain diseases.

How does Helen M. Mcrae approach personalized genetic counseling and testing for patients?

Helen M. Mcrae takes a personalized approach to genetic counseling and testing, considering each patient's unique medical history, family background, and specific concerns to tailor recommendations and interventions that are most relevant and beneficial to them.

What can patients expect during a genetic counseling session with Helen M. Mcrae?

During a genetic counseling session with Helen M. Mcrae, patients can expect to discuss their personal and family medical history, receive education about genetic conditions, explore testing options, understand the implications of genetic information, and receive guidance on managing their genetic risks effectively.

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