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Medical Geneticist

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Nicholas S. Pachter

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Subiaco

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Services Offered by Nicholas S. Pachter

  • Lynch Syndrome

  • Micrognathia

  • Addison's Disease

  • Bannayan-Riley-Ruvalcaba Syndrome

  • Breast Cancer

  • Cardiomyopathy

  • Colorectal Cancer

  • Congenital Heart Disease (CHD)

  • Cowden Syndrome

  • Cramp-Fasciculation Syndrome

  • Ehlers-Danlos Syndrome (EDS)

  • Endocardial Fibroelastosis

  • Endometrial Cancer

  • Familial Colorectal Cancer

  • Giant Mammary Hamartoma

  • Increased Head Circumference

  • Lhermitte-Duclos Disease

  • Li-Fraumeni Syndrome

  • Meier-Gorlin Syndrome

  • Ovarian Cancer

  • Prostate Cancer

  • Protein Deficiency

  • Trichohepatoenteric Syndrome

  • Trichorrhexis Nodosa

  • Turcot Syndrome

About Of Nicholas S. Pachter

Nicholas S. Pachter is a male medical professional who helps people with various health conditions like Lynch Syndrome, Micrognathia, and Addison's Disease. He also supports patients with different types of cancer, heart diseases, and genetic disorders like Cowden Syndrome and Ehlers-Danlos Syndrome.

Nicholas S. Pachter uses special skills and treatments to care for his patients. He is good at communicating with them, making sure they understand their conditions and treatment options. Patients trust him because he listens to their concerns and provides compassionate care.

To stay updated with the latest medical knowledge, Nicholas S. Pachter reads research papers and attends conferences. This helps him offer the best care to his patients. He also collaborates with other medical professionals to share knowledge and improve patient outcomes.

Nicholas S. Pachter's work has positively impacted many patients' lives. For example, his research on genetic carrier screening has helped couples make informed decisions about starting a family. He is currently involved in a clinical trial called "Mackenzie's Mission" to improve reproductive carrier screening practices.

One of Nicholas S. Pachter's notable publications is "Nationwide, Couple-Based Genetic Carrier Screening" in The New England Journal of Medicine. This shows his commitment to advancing medical knowledge and improving patient care.

In summary, Nicholas S. Pachter is a dedicated and skilled medical professional who cares for patients with a wide range of health conditions. His commitment to staying updated with the latest research and collaborating with colleagues ensures that his patients receive high-quality care.

Publications by Nicholas S. Pachter

Clinical Trials by Nicholas S. Pachter

Mackenzie's Mission: The Australian Reproductive Carrier Screening Project

Enrollment Status: Active not recruiting

Published: April 09, 2024

Intervention Type: Other

Study Drug:

Study Phase: Not Applicable

Frequently Asked Questions About Nicholas S. Pachter

What conditions does Nicholas S. Pachter specialize in as a Medical Geneticist?

Nicholas S. Pachter specializes in diagnosing and managing genetic disorders and conditions that have a hereditary component.

How can I benefit from seeing Nicholas S. Pachter as a Medical Geneticist?

By consulting with Nicholas S. Pachter, you can receive personalized genetic counseling, risk assessment, and guidance on genetic testing options.

What types of genetic testing does Nicholas S. Pachter offer?

Nicholas S. Pachter offers a range of genetic tests, including diagnostic testing, carrier screening, predictive testing, and prenatal testing.

How can I prepare for a genetic counseling session with Nicholas S. Pachter?

To prepare for a genetic counseling session, gather your family medical history, list any questions or concerns you have, and be ready to discuss your personal health history.

Can Nicholas S. Pachter help me understand my risk of developing a genetic condition?

Yes, Nicholas S. Pachter can assess your risk of developing a genetic condition based on your family history, personal health information, and genetic testing results.

What should I expect during a consultation with Nicholas S. Pachter?

During a consultation with Nicholas S. Pachter, you can expect a thorough evaluation of your medical history, discussion of genetic testing options, interpretation of test results, and personalized recommendations for managing your genetic health.

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