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Prolactinoma

Endocrine Diseases

Prolactinoma

More information will be added to this page in time.

For more information, please refer to:

  • RARE Portal: Pituitary Conditions
  • Australian Pituitary Foundation
  • Fact Sheet: A Guide to Prolactinoma (Australian Pituitary Foundation)
  • National Organization for Rare Disorders (NORD): Prolactinoma
  • Genetic and Rare Diseases (GARD) Information Center: Prolactinoma

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Cushing’s Disease
Corpus Callosum Disorders (CCD) (Group of Conditions)

 

DISCLAIMER: The information on the Rare Awareness Rare Education (RARE) Portal is intended for educational purposes only and does not replace professional advice.  

Rare diseases typically display a high level of symptom complexity and variability. Individuals diagnosed with the same rare disease may be impacted differently and each person’s experience is unique.  Please seek support from qualified healthcare professionals to learn more about the most suitable care and support options for you.  See our Terms of Use for more information.

Development of the RARE Portal has been funded by the Australian Government and is one of the key deliverables of the National Strategic Action Plan for Rare Diseases.

 

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  • Information
    • About
    • What Is A Rare Disease?
    • Commonly Used Terms In Rare Disease 
    • Rare Disease Classifications
    • Importance of Early Diagnosis in Rare Disease
    • Information on Genetic Services
    • Disability Support Information
    • Personalised tools suitable for rare disease
  • Community
    • Rare Disease Community
      • Mental Health and Wellbeing Support
    • Researchers
    • Healthcare Professionals
      • Supporting the Mental Health and Wellbeing of People Living with a Rare Disease
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    • A-Z Rare Diseases
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Rare Voices Australia acknowledges Aboriginal and Torres Strait Islander people as the Traditional Owners of Country throughout Australia and as a priority population of the rare disease sector. We pay our respects to Elders–past, present and emerging.

 

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The RARE Portal is a living website with new information added regularly. You can contact the RARE Helpline for service navigation support.

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