Gareth S. Baynam

Geneticist

Male📍 Crawley

About of Gareth S. Baynam

Gareth S. Baynam is a geneticist based in Crawley, Western Australia, working from 35 Stirling Hwy, Crawley WA 6009. Genetics can play a big part in how people grow, how their body develops, and why some health problems happen. Gareth’s work looks at the link between genes and real-life symptoms, so families can make more sense of what’s going on.

In many cases, this kind of care helps when there are complex or rare conditions in the family. Gareth supports people who need help understanding issues such as developmental differences, learning and behavioural needs, and changes in how the body forms. That can include things like autism spectrum traits, cerebral palsy, epilepsy, and problems with movement and muscle tone at different stages of life.


Genetic conditions can also involve the skin, face, and body shape. At times, people are referred when there are signs like distinctive facial features, changes in head size, cleft lip or palate, or other differences in growth. There are also syndromes where the skin, hair, or nails are affected, and where careful checking helps guide next steps.

Some patients are seen because of gut and feeding problems too. Examples in Gareth’s practice include conditions like achalasia and oesophageal issues, as well as birth defects such as gastroschisis. Others may come in with endocrine or growth concerns, including things like hormonal or growth-related conditions, and problems that affect weight and development.


Not all genetic work is about development. Some conditions also affect organs and cancer risk. In Gareth’s practice, this can include conditions linked to testicular cancer, and other inherited changes that may need ongoing monitoring. There are also connective-tissue and immune-related conditions, where the goal is to work out what’s driving the symptoms and what needs follow-up.

People may also be referred when there are heart or body-wide concerns, including certain syndromes that involve facial, heart, and skin features. The aim is to bring the pieces together in a way that’s clear and practical for families.


Details about education and years of experience aren’t listed here. What is clear is that Gareth’s practice covers a wide range of genetic conditions, and the focus stays on making sense of genetic results and supporting care planning. Clinical trial details aren’t listed, but the service is built around helping families understand genetics in the real world.

Services & Conditions Treated

Peutz-Jeghers SyndromeBreast Enlargement In MalesCardiofaciocutaneous SyndromeCortical DysplasiaCostello SyndromeHypotoniaIncreased Head CircumferenceMelasmaRussell-Silver DwarfismSertoli-Leydig Cell TumorAchalasia Microcephaly SyndromeAchard SyndromeAcrofacial Dysostosis Rodriguez TypeAcrofrontofacionasal Dysostosis SyndromeAcromicric DysplasiaAplasia Cutis CongenitaArachnodactylyAutism Spectrum DisorderAutosomal Recessive Cutis Laxa Type 1Beckwith-Wiedemann SyndromeBilateral Perisylvian PolymicrogyriaCerebral PalsyCleft Lip and PalateClouston SyndromeCornelia De Lange SyndromeCraniosynostosisCrouzon SyndromeCutis LaxaEctodermal DysplasiasEpilepsyEsophageal AtresiaFamilial HypercholesterolemiaFetal Alcohol Syndrome (FAS)Focal or Multifocal Malformations in Neuronal MigrationFrontonasal DysplasiaGastroschisisGigantismHerniaHypospadiasImmune Defect due to Absence of ThymusKabuki SyndromeLamellar IchthyosisMacroglossiaMetopic RidgeMicrocephalyMicrognathiaMosaicismNonbullous Congenital Ichthyosiform ErythrodermaOsteopetrosisOsteosclerosis Autosomal DominantPeriventricular HeterotopiaPierre Robin SequencePlagiocephalyPneumoniaRASopathiesSepto-Optic DysplasiaSpastic Diplegia Infantile TypeSplit Hand Foot MalformationTesticular CancerTreacher Collins SyndromeTrichohepatoenteric SyndromeTrichorrhexis Nodosa

Publications

1 total

Septo-optic dysplasia and gastroschisis: trends in birth prevalence and association with maternal age.

European journal of pediatrics • December 06, 2024

Frequently Asked Questions

What services does Dr Gareth S. Baynam offer?
Dr Baynam is a geneticist who offers services related to a wide range of genetic conditions and syndromes, including Peutz-Jeghers Syndrome, Beckwith-Wiedemann Syndrome, Cornelia De Lange Syndrome, Kabuki Syndrome, RASopathies and many others listed in his practice offerings.
Which conditions are a focus of his work?
His focus covers developmental, craniofacial, neural and metabolic conditions among others, such as autism spectrum disorders, cerebral palsy, cleft lip and palate, microcephaly, facial dysostosis syndromes, and various chromosomal or genetic disorders noted in the service list.
Where is Dr Baynam based?
He practices at 35 Stirling Highway, Crawley, WA 6009, Australia.
What is Dr Baynam’s professional title?
He is a Geneticist.
What kind of genetic issues might patients bring to a consultation with him?
Patients might seek assessment or management related to conditions such as autosomal recessive and dominant disorders, craniofacial anomalies, growth and developmental concerns, epilepsy, epilepsy-related migrational disorders, and the many syndromic conditions listed in his services.

Contact Information

35 Stirling Hwy, Crawley, WA 6009, Australia

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