Tony Roscioli

Clinical Geneticist

Male📍 Sydney

About of Tony Roscioli

Tony Roscioli is a Clinical Geneticist working in St. Vincent's Clinical School, Sydney, NSW 2052, Australia. His work focuses on helping families understand genetic conditions, especially when children are born with differences in growth, development, or body structure.


Genetic problems can be complex, and the starting point is often the same: puzzling symptoms, unanswered questions, and a need for clear, practical answers. In many cases, Tony looks at how changes in genes may explain what’s going on and what it could mean for the person and their family.


People seek genetic help for a range of conditions. This can include craniofacial and bone conditions such as craniosynostosis, Crouzon syndrome, Saethre-Chotzen syndrome, and cleft lip and palate. At times, families also come in for concerns around limb and skin findings, including things like cleidocranial dysplasia or skin conditions that run in families.


Tony also supports patients with neurodevelopmental and neurological concerns. This can involve issues like seizures, movement disorders, muscle weakness, and developmental conditions that affect how the brain grows and works. Some families are looking at epilepsy in children, while others are dealing with longer-term neurological patterns.


There are also genetic conditions affecting hearing, vision, and growth. For example, families may ask about hearing loss or optic nerve issues. Growth and development concerns can include short stature and syndromes linked with hormone or body-wide differences.


Some referrals focus on immune and blood-related conditions too. This may include primary immunodeficiency, as well as certain blood disorders that can show up early in life. In other cases, the concern is about how the body processes food and energy, like metabolic conditions, or how the gut works, such as issues seen in infants.


Where possible, Tony helps connect the dots between symptoms and likely genetic causes. That can also support planning for the future, including what extra checks might be useful and how other family members may be affected.


Education details for Tony Roscioli aren’t listed here, and neither are specific years of experience. Clinical trial involvement also isn’t provided in the information available. If you’d like, the clinic can usually share more about his background and current services when you enquire.

Services & Conditions Treated

CraniosynostosisCrouzon SyndromeBlepharocheilodontic SyndromeCoffin-Siris SyndromeFukuyama Type Muscular DystrophyLissencephalyMetopic RidgeMiller SyndromeMuenke SyndromePlagiocephalyWalker-Warburg SyndromeX-Linked Retinal DysplasiaAcanthosis NigricansAchalasia Microcephaly SyndromeAcheiropodyAcromicric DysplasiaAcute Cerebellar AtaxiaAplasia Cutis CongenitaArthrogryposis Multiplex CongenitaBrachydactyly Mononen TypeCantu SyndromeChondrodystrophyCleft Lip and PalateCleidocranial DysplasiaClouston SyndromeCongenital ContracturesCortical DysplasiaCramp-Fasciculation SyndromeCutis LaxaDeafness Craniofacial SyndromeDrug Induced DyskinesiaEctodermal DysplasiasEctropionEpilepsyEpilepsy in ChildrenFarber LipogranulomatosisFetal Akinesia SequenceFetal Enterovirus SyndromeGastroesophageal Reflux in InfantsGerodermia OsteodysplasticaGlucose Phosphate Isomerase DeficiencyHallervorden-Spatz DiseaseHearing LossHepatic Venoocclusive Disease with ImmunodeficiencyHirsutism in WomenHypotoniaKBG SyndromeLactic AcidosisLambdoid SynostosisLeigh SyndromeLeukodystrophyLipogranulomatosisMeier-Gorlin SyndromeMelasmaMicrocephalyMicrognathiaMosaicismMovement DisordersOptic Nerve AtrophyPerrault SyndromePneumocystis Jiroveci PneumoniaPontocerebellar HypoplasiaPrader-Willi SyndromePrimary Immunodeficiency (PID)Primary Lateral SclerosisRett SyndromeSaethre-Chotzen SyndromeSchwartz-Jampel SyndromeSeizuresShort Stature (Growth Disorders)Sideroblastic AnemiaSpasmus NutansSpastic Paraplegia Type 2Spastic Paraplegia Type 7Spinal Muscular Atrophy (SMA)Spinal Muscular Atrophy Type 3Stickler SyndromeTurner SyndromeUndescended TesticleWest SyndromeX-Linked Lymphoproliferative DiseaseX-Linked Spondyloepiphyseal Dysplasia Tarda

Publications

1 total

Nationwide, Couple-Based Genetic Carrier Screening.

The New England journal of medicine • November 20, 2024

Frequently Asked Questions

What services does Tony Roscioli offer as a clinical geneticist?
Tony Roscioli provides genetic assessment and counselling for a range of congenital and developmental conditions, including craniofacial syndromes, growth disorders, epilepsy with genetic links, and other genetic conditions listed in his service offerings.
Which conditions are commonly discussed with a clinical geneticist like Tony Roscioli?
Conditions may include craniosynostosis, various craniofacial and skeletal syndromes, developmental and neurological conditions, and chromosomal or genetic disorders. Specific conditions are discussed during the assessment based on your family history and clinical findings.
Where are appointments with Tony Roscioli held?
Appointments are at St. Vincent's Clinical School in Sydney, NSW 2052.
How can I prepare for a genetics appointment?
Bring any relevant medical records, family medical history, and previous test results. Your clinician will explain what tests or genetic counselling may be helpful for your situation.
What should I expect during a genetic consultation?
The clinician will review medical and family history, discuss possible genetic causes, outline testing options if appropriate, and talk through the implications for you and your family. Questions are welcome at every step.
Are there specific conditions that Tony Roscioli focuses on?
The listed service areas cover a broad range of genetic and developmental conditions, including many craniofacial, neurological, and developmental syndromes. Your exact concerns will be addressed during the consult.

Contact Information

St. Vincent's Clinical School, Sydney, NSW 2052, Australia

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