Peutz-Jeghers syndrome (PJS) is a genetic condition characterized by development of polyps in the gastrointestinal tract (often in the small intestine), and dark blue or brown spots on the skin (mucocutaneous pigmentation). PJS can affect both males and females.

Below on this page is some information about this condition as well as links to useful resources for Australians living with a rare disease.

Synonyms: PJS, hamartomatous intestinal polyposis, polyps and spots syndrome, intestinal polyposis-cutaneous pigmentation syndrome, periorificial lentiginosis syndrome, Hutchinson Weber-Peutz syndrome.

Universal rare disease classifications provide a common language for recording, reporting and monitoring diseases. Please visit the Rare Disease Classifications page for more information about these internationally recognised classifications.

ORPHA:2869 Peutz-Jeghers syndrome

ICD-11: LD2D.0 Peutz-Jeghers syndrome

Rare diseases typically display a high level of symptom complexity. There is often a wide range of symptoms and the symptoms may vary between individuals in terms of its presentation, severity, duration and impact. Please speak to your medical team to learn more about the symptoms of this condition. 

Rare diseases are often serious and progressive, exhibiting a high degree of symptom complexity, leading to significant disability. Majority of the estimated two million Australians living with a rare disease meet the Australian Government’s definition for disability (in accordance to the Australian Public Service Commission and Australian Bureau of Statistics), and many experience severe and permanent disability impacts. If you or someone you care for is experiencing disability-related impacts from a rare condition, please speak with a health or disability professional for advice. Information about relevant disability support can be found at the RARE Portal’s Disability Support Information page.

PJS is a genetic condition. It is caused by disease-causing genetic changes (variants) in the STK11 gene located on Chromosome 19. All individuals have two copies (alleles) of the STK11 gene – one on each chromosome that is inherited from each parent. PJS is an autosomal dominant condition, which means that having a genetic variant in just one of the STK11 gene copies can result in PJS.

The genetic variant can be inherited, which means it can be passed on to the next generation. If a parent has the autosomal dominant gene variant, there is 50% chance that they will pass that genetic variant to each of their children. More information on autosomal dominant inheritance pattern can be found at Centre for Genetics Education: Autosomal dominant inheritance.

If you would like to learn more about the inheritance and impact of this condition, please ask your doctor for a referral to a genetic counsellor. Genetic counsellors are qualified allied health professionals who can provide information and support regarding genetic conditions and testing. More information about genetic counselling can be found at:

• Information on Genetic Services
• The National and State Services pages underneath the ‘Genetic Counselling’ sections listed

A timely diagnosis is critical for better patient outcomes, the provision of the best possible care and treatment options, access to services and support, increased reproductive confidence and the ability to participate in clinical trials.

Please speak to your medical team to learn more about the available diagnostic pathways for this condition.

Please speak to your medical team to learn more about the possible treatment or management options for your condition. Treatment will depend on an individual’s specific condition and symptoms. It is also important to stay connected to your medical team so that you can be made aware of any upcoming clinical trial opportunities.

Clinical care for rare diseases often involves a multidisciplinary team of medical, care and support professionals. Please note that the information provided here is as a guide and that RVA does not necessarily monitor or endorse specific clinics or health experts.

Healthcare professionals involved in the treatment of PJS may include general practitioners (GP), gastroenterologists, oncologists and others. The need for different healthcare professionals may change over a person’s lifetime and extend beyond those listed here.

If you know of any relevant care guidelines, please let us know via the Contribute page. 

Individuals living with rare diseases may have complex medical issues and disabilities, which are not always visible. It is often useful to refer to their medical history as well as personal information such as a medical card, doctor’s letter, or if available, a rare disease passport, for relevant information.

If you know of any relevant emergency management guidelines or information relevant to emergency care, please let us know via the Contribute page. 

There are specific considerations around participating in rare disease research, including clinical trials. It is important to be mindful of issues such as data privacy, research ethics, consent and differences in research regulations between Australia and other countries.

If you are interested in finding clinical trials for your condition, please visit the following websites; however, there may not be any clinical trials available:

• Australian Clinical Trials
• ClinicalTrials.gov

It is best to discuss your interest in any clinical trials with your medical team to determine suitability and eligibility.

Please note that RVA does not necessarily monitor or endorse each group/organisation’s operational governance and activities.

We are not aware of any rare disease organisations for PJS in Australia or internationally. If you know of any rare disease organisation/s supporting people living with PJS, please let us know via the Contribute page. If you are interested in starting an Australian organisation, please see Engaged, Ethical and Effective: A Guide for Rare Disease Organisation Leaders in Australia.

Please note that RVA does not monitor or endorse each group/organisation’s operational governance and activities. When engaging with a group, please consider the information on the RARE Portal’s Finding Helpful Peer and Community Supports page.

PJS vary between individuals, and each person’s experience is unique.

Personal stories shared with RVA: Matthew’s Story

If you would like to share your personal story with RVA, please visit the Rare Voices Australia: Share Your Story page. RVA will consider your story for publishing on our website and inclusion on the RARE Portal.

For information on available government and social services that provide support for individuals with a rare disease, please visit the National and State Services pages.

People living with a rare disease, including families and carers, often face unique challenges such as diagnostic delays, misdiagnoses, limited treatment options, and limited access to rare disease specialists and support. These challenges may impact people’s emotional wellbeing and quality of life. Many people find it helpful to seek mental health and wellbeing support to cope with ongoing stress and uncertainty. Connecting with people who have shared experiences through a support group may also be helpful. Information about relevant mental health and wellbeing support can be found at:

• Mental Health and Wellbeing Support for Australians Living with a Rare Disease
• The National and State Services pages underneath the ‘Mental Health’ sections listed

Further information on PJS can be found at:

• Cancer Institute NSW: Peutz-Jeghers Syndrome
• Genetic and Rare Diseases (GARD) Information Center: Peutz-jeghers syndrome
• National Organization for Rare Disorders (NORD): Peutz-Jeghers Syndrome

GeneReviews®: Peutz-Jeghers Syndrome

Online Mendelian Inheritance in Man, OMIM®: #175200 Peutz-Jeghers Syndrome; PJS

Orphanet: Peutz-Jeghers syndrome

Human Phenotype Ontology (HPO): Peutz-Jeghers syndrome

This page has been developed by Rare Voices Australia (RVA)’s RARE Portal team. If you would like to see more information added to this page, please reach out via the Contact form. If you would like to share relevant resources for this condition, please visit the Contribute page.

If you are aware of any additional information that may benefit stakeholders with an interest in this page, or if you notice any broken links or inaccurate information, please let us know via the Contribute page.