Tiong Y. Tan

Clinical Geneticist

📍 Melbourne

About of Tiong Y. Tan

Tiong Y. Tan is a Clinical Geneticist based at Flemington Road in Melbourne, VIC, Australia.


Genetics can explain why some babies and children grow and develop in a different way. Dr Tan works with families who are dealing with suspected inherited conditions, and also with people who need help making sense of results from genetic testing.


In many cases, the focus is on development and early life changes. This can include delays in speech and learning, slower growth, low muscle tone, or trouble with movement like apraxia. At times, there may also be issues with brain development, such as cortical dysplasia or polymicrogyria, and some families are managing seizures or epilepsy, including absence seizures and generalised tonic-clonic seizures.


There are also families who come in because of changes in body shape and structure. For example, craniofacial differences like Pierre Robin sequence, Treacher Collins syndrome, Crouzon syndrome, and Goldenhar disease can be part of the story. Other signs might involve limb and bone differences, differences in the hands and fingers, or issues like craniosynostosis and metopic ridge.


Heart problems can also be part of the genetic picture. Dr Tan looks after patients where genetic conditions are linked with heart muscle disease, including hypertrophic cardiomyopathy (HCM) and restrictive cardiomyopathy (RCM).


Some conditions involve the digestive system, too, such as achalasia or oesophageal atresia. Other areas can include skin and hair changes, hormone or reproductive differences, and conditions affecting the immune system or metabolism, like VLCAD deficiency. Genetic mosaicism may also come up in discussions, where test results show changes in some cells but not all.


Genetic testing is only one piece of care. Dr Tan also helps families understand what results can mean for health now, and what to watch for over time. Keeping up with new genetics knowledge matters in this field, even though the details of research or clinical trials aren’t listed here.


When a condition is complex, it helps to have someone who can explain it clearly, break things into manageable steps, and support families through decisions that can feel overwhelming.

Services & Conditions Treated

MicrognathiaAchalasia Microcephaly SyndromeAicardi-Goutieres SyndromeCampomelia Cumming TypeCampomelic DysplasiaCortical DysplasiaDelayed GrowthDevelopmental Expressive Language DisorderEarly Infantile Epileptic EncephalopathyKBG SyndromeKoolen De Vries SyndromeMicrocephalyMultiple Synostoses Syndrome 1Pierre Robin SequenceRommen Mueller Sybert SyndromeAbsence SeizureAcrofacial Dysostosis Rodriguez TypeAcrofrontofacionasal Dysostosis SyndromeAdenosine Monophosphate Deaminase DeficiencyAplasia Cutis CongenitaApraxiaBrachydactyly Mononen TypeCardiofaciocutaneous SyndromeCardiomyopathyClouston SyndromeCoffin-Siris SyndromeCostello SyndromeCraniosynostosisCrouzon SyndromeDeafness Craniofacial SyndromeDysarthriaDyskeratosis CongenitaEctodermal DysplasiasEsophageal AtresiaFamilial Multiple LipomatosisFocal or Multifocal Malformations in Neuronal MigrationFrontonasal DysplasiaGeneralized Tonic-Clonic SeizureGenital DwarfismGoldenhar DiseaseHypertrophic Cardiomyopathy (HCM)HypospadiasHypotoniaIncreased Head CircumferenceIntersexKuster SyndromeMayer-Rokitansky-Kuster-Hauser SyndromeMetopic RidgeMicrocephaly Deafness SyndromeMiller SyndromeMosaicismMullerian AplasiaNoonan SyndromePectus CarinatumPlagiocephalyPolymicrogyriaPontocerebellar HypoplasiaPremature Ovarian FailureRASopathiesRestrictive Cardiomyopathy (RCM)Saethre-Chotzen SyndromeSeizuresTeratoma of the MediastinumTotal Anomalous Pulmonary Venous ReturnTreacher Collins SyndromeUndescended TesticleVery Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency

Publications

1 total

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.

medRxiv : the preprint server for health sciences • April 16, 2025

Frequently Asked Questions

What services does Dr Tiong Y. Tan provide as a Clinical Geneticist?
Dr Tan specialises in clinical genetics, helping to diagnose and manage genetic conditions. His areas span a wide range of syndromes and features listed in his practice list.
Which conditions do you commonly work with?
He works with conditions such as microcephaly syndromes, developmental and language concerns, various facial and skeletal syndromes, epilepsy-related disorders, and many other genetic issues listed in his care focus.
Who can see you for a consult?
Appointments are for patients needing genetic assessment, including children and adults, to understand possible genetic causes of their health concerns.
Where are you located and how can I book an appointment?
Consultations are in Melbourne, at Flemington Road, VIC. To book, contact the clinic or use the practice’s usual appointment channels.
What should I expect at my first visit?
At the first visit, the doctor will review medical history, family history, and any prior tests. They may discuss possible genetic testing options and what the results could mean for care.
Do you provide genetic testing and how are results explained?
Genetic testing may be discussed as part of the assessment. If testing is done, the results will be explained in plain terms, with emphasis on what the findings mean for management and future care.
What concerns should I prepare for my appointment?
Gather your medical records, any prior genetic or imaging results, and a list of current symptoms and medications. If you have a family history of genetic conditions, note it down as well.

Contact Information

Flemington Road, Melbourne, VIC, Australia

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