Ashley Hertzog

Metabolic Geneticist

📍 Westmead

About of Ashley Hertzog

Ashley Hertzog is a Metabolic Geneticist based in Westmead, NSW 2154. Their work is in the “metabolism and genes” space, where small changes in how the body makes or uses energy can affect growth, the brain, and overall health.


In practice, this kind of care often looks after people who have rare inherited conditions. That can include problems with the urea cycle, which helps the body get rid of ammonia. Over time, these issues can lead to metabolic problems and episodes where the body struggles to clear waste properly.


Ashley also helps with conditions linked to enzyme and metabolic pathways. Some examples are 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency and Ornithine Transcarbamylase Deficiency. Others include Orotic Aciduria Type 1 and Smith-Lemli-Opitz Syndrome. These conditions can show up in childhood, but they can also be recognised later, depending on symptoms and how the illness progresses.


There are also genetic metabolic conditions that come with wider body effects. For instance, CACH syndrome and acromicric dysplasia can affect how the body develops, including features like growth and body shape. Metabolic acidosis is another key area. It’s when the body becomes too acidic, and it can be serious if it isn’t managed quickly.


Because these conditions are often uncommon, the approach usually needs clear thinking and steady support. Ashley works with families and clinicians to make sense of symptoms, test results, and what can happen next. In many cases, the goal is to catch problems early and help reduce the risk of complications.


For some patients, care can also involve looking at physical signs that may connect to a genetic condition. Syndactyly can be one such sign, depending on the overall picture. The exact plan varies a lot from person to person, and that’s normal with metabolic genetic conditions.


Education and training details aren’t listed here, so it’s best to confirm any specific degrees or study history directly through the clinic. If research or trials are relevant, those details are also not shown in the information provided.


You can find Ashley in Westmead, where metabolic genetic care is closely tied to hospitals and specialist services. If you’re looking for help with suspected or confirmed metabolic genetic conditions, this is the kind of specialist support that can make a big difference.

Services & Conditions Treated

3-Hydroxy-3-Methylglutaryl-CoA Lyase DeficiencyOrnithine Transcarbamylase DeficiencyOrotic Aciduria Type 1Acromicric DysplasiaCACH SyndromeMetabolic AcidosisSmith-Lemli-Opitz SyndromeSyndactylyUrea Cycle Disorders (UCD)

Publications

1 total

Treatment of HMG-CoA Lyase Deficiency-Longitudinal Data on Clinical and Nutritional Management of 10 Australian Cases.

Nutrients • December 04, 2022

Frequently Asked Questions

What services does Dr Ashley Hertzog offer?
Dr Ashley Hertzog works as a Metabolic Geneticist and focuses on conditions such as 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Ornithine Transcarbamylase Deficiency, Orotic Aciduria Type 1, Acromicric Dysplasia, CACH Syndrome, Metabolic Acidosis, Smith-Lemli-Opitz Syndrome, Syndactyly, and Urea Cycle Disorders. If you’re unsure whether a condition fits, ask at your appointment.
Where is Dr Hertzog located for appointments?
Appointments are available in Westmead, NSW 2154, Australia.
Who should consider seeing a Metabolic Geneticist like Dr Hertzog?
People who have or suspect metabolic disorders or genetic conditions such as Urea Cycle Disorders or other listed metabolic conditions, and families seeking guidance on diagnosis and management.
What should I bring to a first appointment?
Bring any relevant medical records or test results related to your condition, and a list of current medications. If you’re unsure what to bring, contact the clinic before your visit.
How can I book or arrange an appointment?
Contact the clinic at the Westmead location to arrange an appointment. If you have questions about coverage or eligibility, ask when you call.
What topics are typically discussed in these consultations?
Discuss the diagnosis, treatment options, management plans, and any concerns about the listed metabolic conditions or genetic issues. The aim is to help families understand and manage the condition.