Zornitza Stark

Geneticist

📍 Melbourne

About of Zornitza Stark

Zornitza Stark is a Geneticist based on Flemington Road in Melbourne, VIC, Australia.


Genetics can be confusing, especially when it affects a child’s growth, learning, or health. Zornitza looks after families who need answers about how a condition may run in a family, or why it has shown up in the first place.


Many people who see a geneticist have questions about rare or complex conditions. These can include genetic disorders that affect the face and bones, hearing, brain development, and body movement. Some families come in because of health issues that may look different from one person to another, even within the same family.


In many cases, the focus is on helping work out what’s going on and what it might mean going forward. This can involve looking at things like developmental delay, epilepsy and other seizure types, abnormal muscle tone, and problems with how the body uses energy or breaks down certain substances. At times, appointments also cover conditions related to the kidneys, liver, or hormones, along with differences in head size or shape.


Genetic information can also help with planning. It may guide next steps for treatment support, referrals, and what to watch for as a child grows. Zornitza’s approach stays practical and patient. It’s about making sense of results in plain language, and helping families feel less lost after the appointments.


If you’re dealing with ongoing health concerns, you might be trying to connect the dots. That’s where a geneticist can be helpful. Zornitza works with families to understand the bigger picture, not just the one symptom that brought you in.


While genetics testing can be a big step, it doesn’t always have to be scary. Zornitza aims to keep the conversation calm and clear, so you know what’s being considered and why. The goal is to support families in Melbourne with answers, clarity, and next-step thinking.

Services & Conditions Treated

Cockayne Syndrome Type 1KBG SyndromeMicrognathiaSaethre-Chotzen SyndromeAcrocephalopolydactylyAcromicric DysplasiaApert SyndromeCardiofaciocutaneous SyndromeCockayne SyndromeCockayne Syndrome Type 2Cortical DysplasiaCraniosynostosisEEC SyndromeHypotoniaLeukodystrophyMeningococcemiaMicrocephaly Deafness SyndromeMyoclonic EpilepsyPerrault SyndromePfeiffer SyndromeRiboflavin Transporter Deficiency NeuronopathySotos SyndromeSyndactylyWest SyndromeAchalasia Microcephaly SyndromeAcrofacial Dysostosis Catania TypeAcrofacial Dysostosis Rodriguez TypeAcrofrontofacionasal Dysostosis SyndromeAdenosine Monophosphate Deaminase DeficiencyAplasia Cutis CongenitaAutism Spectrum DisorderAxenfeld-Rieger SyndromeBartter SyndromeBlue Cone MonochromatismChoanal AtresiaCholesteryl Ester Storage DiseaseChronic Kidney DiseaseClouston SyndromeColobomaColor BlindnessCongenital Central Hypoventilation SyndromeCongenital Diaphragmatic HerniaCornelia De Lange SyndromeCostello SyndromeCrouzon SyndromeDelayed GrowthDiaphragmatic HerniaDrug Induced DyskinesiaEctodermal DysplasiasEpilepsyEpilepsy in ChildrenFebrile NeutropeniaFragile X SyndromeGeneralized Tonic-Clonic SeizureGenetic Epilepsy with Febrile Seizures Plus (GEFS+)GigantismHearing LossHerniaHirsutism in WomenHydroceleHypercalcemiaIncreased Head CircumferenceInfant Epilepsy with Migrant Focal CrisisInfantile Axonal NeuropathyIntersexIntrauterine Growth RestrictionIridogoniodysgenesis Type 1Lactic AcidosisLeigh SyndromeLennox-Gastaut Syndrome (LGS)Liver FailureMeckel's DiverticulumMetabolic AcidosisMetopic RidgeMicrocephalyMilk-Alkali SyndromeMiller SyndromeMosaicismMovement DisordersOmphaloceleOsteopetrosisOsteosclerosis Autosomal DominantPeripheral NeuropathyPlagiocephalyPolycystic Kidney DiseasePolymicrogyriaPontocerebellar HypoplasiaPremature Ovarian FailurePrimary Lateral SclerosisRASopathiesSeizuresSideroblastic AnemiaSplit Hand Foot MalformationStrokeTreacher Collins SyndromeTurner SyndromeUmbilical HerniaUndescended TesticleVery Long-Chain Acyl-CoA Dehydrogenase (VLCAD) DeficiencyWiedemann-Steiner SyndromeWilliams SyndromeWolman Disease

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 Zornitza Stark offer?
Dr Stark works as a geneticist and can assess a range of genetic conditions. Her listed services include diagnosing and advising on various syndromes and conditions such as Cockayne syndrome, Crouzon syndrome, Sotos syndrome, Apert syndrome and many others. If you’re unsure whether a condition is covered, contact the clinic to check.
Which conditions might be considered for a genetic consult?
Genetic consultations may be considered for concerns like developmental delay, congenital anomalies, sensory impairments, epilepsy with a possible genetic link, growth concerns or multiple family members with similar features. The doctor will review your individual history to determine relevance.
How do I book an appointment with Dr Stark?
To arrange an appointment, contact the clinic in Melbourne. The exact address is Flemington Road, Melbourne, VIC. The staff can guide you through appointment times, referral requirements and any preparation needed.
What should I bring to a genetic appointment?
Bring any relevant medical records, including prior test results, imaging reports and family medical history. If you have a referral from a GP or specialist, bring that too so the team can prepare appropriately.
Is this service suitable for children or adults?
Genetic clinics often see both children and adults with suspected or confirmed genetic conditions. Discuss your age and concerns when booking to ensure the right setting and expertise for your visit.
What language is used in consultations?
Consultations are conducted in plain English. If you require interpreter support, ask when booking to arrange appropriate arrangements.

Contact Information

Flemington Road, Melbourne, VIC, Australia

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