Kelly L. Rogers

Medical Geneticist

📍 Parkville

About of Kelly L. Rogers

Kelly L. Rogers is a Medical Geneticist based in Parkville, VIC 3052. She looks after people who need help understanding genes and how they can affect health across families. Genetics can feel a bit overwhelming at first, especially when you’re dealing with real-life symptoms, so she aims to keep the conversation clear and steady.


In her work, she supports patients with both inherited and genetic-related conditions. This can include rare syndromes and changes seen in early development, as well as medical issues that show up later. At times, her patients may be dealing with things like congenital conditions, inherited hormone and metabolism problems, or disorders that affect muscles and nerves. She also works with families where there’s concern about cancer risk, and situations involving eye or skin findings.


She may also be involved when testing links to conditions such as familial polyposis, or lipid related problems in the family. In some cases, the goals are to sort out what’s going on, work out what it means for other family members, and talk through next steps. Genetics doesn’t always give instant answers, but it can make the picture less blurry over time.


Over time, Kelly’s experience covers a broad range of genetic conditions, from specific named syndromes to longer-term health questions. Her training in medical genetics helps her work through the process of genetic testing, then explain results in a way that makes sense for everyday life. Research and clinical trials information isn’t listed here, but her approach stays focused on practical care, family support, and making sure people know what options are available.

Services & Conditions Treated

Grix Blankenship Peterson SyndromeOhdo Syndrome, Say-Barber-Biesecker-Young-Simpson VariantAbetalipoproteinemiaAmyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease)BlepharophimosisCongenital HypothyroidismFamilial Adenomatous PolyposisFamilial HypobetalipoproteinemiaHead LiceHypermobile JointsHypolipoproteinemiaLung MetastasesMalariaPrimary Lateral SclerosisRommen Mueller Sybert SyndromeToxoplasmosis

Publications

1 total

Loss of KAT6B causes premature ossification and promotes osteoblast differentiation during development.

Developmental biology • October 30, 2024

Frequently Asked Questions

What services does Dr Kelly L. Rogers offer?
Dr Kelly L. Rogers is a Medical Geneticist in Parkville, VIC. Her work involves genetic assessment and management for various genetic conditions, including disorders such as Grix Blankenship Peterson Syndrome, Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant, Abetalipoproteinemia, and others listed in her service areas.
Which conditions can she help diagnose or manage?
She can help with conditions from her listed service areas, such as Grix Blankenship Peterson Syndrome, Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant, Abetalipoproteinemia, Amyotrophic Lateral Sclerosis (ALS), Blepharophimosis, Congenital Hypothyroidism, Familial Adenomatous Polyposis, Familial Hypobetalipoproteinemia, Hypermobile Joints, Hypolipoproteinemia, Rommen Mueller Sybert Syndrome, and Primary Lateral Sclerosis, among others.
How do I book an appointment with her?
To arrange an appointment, please contact her clinic in Parkville, VIC 3052, Australia. They can provide details on available slots and the booking process.
Where is the clinic located?
The practice is in Parkville, Victoria, Australia (Parkville, VIC 3052).
What languages are used for consultations?
Language details aren’t listed in the profile, so please check with the clinic about available languages for consultations.
Is Dr Rogers currently accepting new patients?
Clinic availability can change. Please contact the Parkville clinic directly to confirm whether new patients are being accepted at this time.