ÐÇ¿ÕÌåÓý

This clinic is responsible for the diagnosis, management and genetic counselling of children with a known or possible genetic condition.

Complex referrals or cases where a child is already a regular patient at Sydney Children’s Hospital, Randwick, will be considered.

Out-of-area referrals for initial diagnosis of uncomplicated genetic conditions will be directed to the genetics service of the patient's local health district.

Referrals are triaged by a member of the clinical genetic team and allocated to either a telehealth appointment or a face-to-face appointment at the appropriate clinic. A genetic counsellor may contact new patients before their clinic visit for previous medical information and results.

Incorrect referrals or insufficient information will be returned to the referring doctor. Requests to see a specific geneticist can be considered but are not always possible.

Clinic function: Diagnosis, assessment and genetic counselling of children with a suspected or confirmed rare genetic or chromosomal diagnosis, multiple congenital anomalies, dysmorphic features and/or intellectual disability.

Location:

• Children: Outpatient department, level 0, Sydney Children’s Hospital, Randwick
• Young adults: Bright Alliance building, level 7, corner of Avoca and High Street 

Advice and guidance for healthcare professionals:

Email service is for health care professionals managing patients and families with known or possible genetic conditions within the Sydney Children’s Hospital, Randwick, South Eastern Sydney Local Health

• Please email [email protected]
• This email is for non-urgent advice and guidance only
• A genetic counsellor will triage your request and provide written advice within 1-2 business days
• Please ensure that you have provided us with your best available contact number in case we need to call you back
• This email account is not checked on weekends or public holidays. 

Urgent referrals: Phone the hospital switchboard on (02) 9382 1111 and ask to page the on-call genetics fellow, clinical geneticist or genetic counsellor. 

The Kids Cancer genetics clinic provides care for children and adolescents with a suspected or known increased genetic risk of tumours and/or cancer.

The clinic team is responsible for diagnosis, genetic counselling, risk assessment, ongoing management and surveillance to support a holistic, child and family-centred approach to care.

The clinic is part of the Kids Cancer Centre. We see children and adolescents in the outpatient clinic on C2North, located on Level 2 Sydney Children’s Hospital Randwick.

• Email: [email protected]
• Phone: 9382 1730

The prenatal clinic is for women and their partners with a personal or family history of an inherited condition, fetal abnormality that may be a genetic disorder, or high-risk results on aneuploid screening.

We provide counselling and facilitate genetic testing and prenatal diagnosis, including Chorionic villus sampling (CVS) and amniocentesis.

Thalassaemia referrals:

Please order FBC, HbEPG, iron studies in both partners. Only refer to genetics if abnormalities are identified in both.

Referral indications include:

• increased-risk aneuploidy results on screening
• diagnosis or suspected fetal abnormality
• personal or family history of a chromosomal/genetic condition
• couples at increased reproductive risk (eg both known carriers of a recessive condition, consanguinity). 

We do not accept referrals for:

• teratogen, please refer to
• couples or individuals for reproductive carrier screening (currently available through GPs, obstetricians, private genetic counsellors and some women’s ultrasound services)
• individuals who have had (or are considering) ‘direct to consumerâ€� genetic testing
• individuals who have had (or are requesting) genetic testing relating to paternity. 

Include in referral:

• EDD/LMP
• investigations/treatment to date
• significant medical and family history
• any relevant social information
• an indication for the preferred language if an interpreter is required

Clinic details: 

• Hours: Tuesdays, 9:30 am -12:30pm
• Location: Maternal-Fetal Medicine Unit, Royal Hospital for Women, Randwick
• Phone: (02) 9382 6042
• Email: [email protected]

The service provides regular outreach clinics to children and adults at Wollongong Hospital. A local genetic counsellor is available for all enquiries.

Please note: There is no administration support, there may be a delay in returning voicemail or email enquiries. If the matter is urgent, please get in touch with the on-call genetics fellow or genetic counsellor (see The General Paediatrics Genetics clinic). 

Contact: 

• Private Mail Bag 8808 SCMC NSW 2521
• Location: Wollongong General Genetics Service, level 2, block C, Wollongong Hospital
• Phone: (02) 4253 4267
• Email: [email protected]

You've been referred to a clinical genetics service at the hospitals. You may already know your family has a genetic condition and want more information or wonder if someone in your family has a genetic condition.

At your appointment, we will talk with you about genetic conditions and do our best to answer any questions you have.

One of our genetic counsellors may contact you by phone or email to gather more information. For example, they may ask about your family health history to help us understand more about your/your child’s health conditions and how we can best support you and your family.

The appointment may be face-to-face or by confidential video link (telehealth).

Please bring your child’s “Blue Book� (Personal Health Record book), any specialist letters or relevant health information, and a Medicare card, if you have one.

Let us know if you want to invite a family member or friend. Feel free to bring a list of questions with you.

At the appointment, you'll see a genetic doctor and/or a genetic counsellor.

We sometimes have medical students or doctors and genetic counsellors in training; we will ask you if it is ok for them to join the appointment.

The appointment will last about 1 hour. We'll discuss your family history and you/your child’s health. We may examine you and/or your child. If you say it is ok, we may take photographs for the medical record.

We will discuss genes and how they can be linked to health problems. We can also explain any tests we recommend and what the results could mean.

We understand you might be worried about your or your child’s health. We will do our best to answer your questions and provide support. We offer tests if we think it could help with your/your child’s health care. But it is your choice. You do not have to have a genetic test if you do not think it is right for you, or your child.

At the end of the appointment, we can talk about the next steps for you/your child or your family.

Genetic testing

We provide tests if we believe they could benefit your or your child’s healthcare. However, the decision is entirely yours. You are not required to have a genetic test if you do not think it is right for you or your child.

If you decide that a genetic test is suitable, we may give you a form for a blood test. This can be done at the hospital’s blood-taking service, where staff are trained to collect blood from both children and adults.

In some cases, a saliva (spit) sample may be taken instead of blood.

We will write to your doctor(s) after the genetics appointment. It will include a summary of the patient's health issues, any planned tests, the results of tests, and helpful resources.

The letter may include information about any planned future visits with the genetics service. We often send you a copy of the letter too.

Taking part in research is your choice If you do not want to take part it is okay to say no. 

This will not impact your health care or your relationship with us.

Research helps us learn about how to give the best care to patients and their families. If there are research studies that may be helpful or interesting for you or your family, we are happy to talk about this more at the appointment. 

Examples of genetics research programs include:

• Registries and databases: Connect patients with the same rare condition, improve understanding of the condition, and link families to clinical trials and support.
• Diagnostic research: For families without a clear diagnosis, further research aims to find a diagnosis and improve care.