Kelan Chen

Geneticist

Male📍 Melbourne

About of Kelan Chen

Kelan Chen is a Geneticist based in Melbourne, VIC, Australia. Kelan looks after people and families who are trying to understand how certain conditions can happen, especially when there may be a genetic link.


In many cases, genetic conditions can show up early in life, or they may be noticed after changes in growth, vision, muscle strength, or breathing. Genetic testing and careful family history can help sort out what’s going on. At times, the answers people get can bring relief. Other times, it can simply help give clearer next steps.


Kelan’s practice includes conditions such as Bosma Arhinia Microphthalmia Syndrome and choanal atresia. These can involve changes around the nose and face, and they may affect how air moves through the nose. There’s also support for people with microphthalmia, where the eyes are smaller than usual.


Kelan also works with families affected by facioscapulohumeral muscular dystrophy (FSHD). FSHD can affect the face, shoulders, and upper arms. Over time, it may cause weakness that becomes more noticeable with certain activities. Having the right diagnosis matters, because it helps families plan and understand what to expect.


Genetics can feel confusing at first. Kelan takes a steady, practical approach, focusing on making complex ideas easier to follow. It’s not just about naming a condition. It’s about looking at the bigger picture, including how a condition may pass through families and what it could mean for relatives.


Because genetic conditions can vary a lot from one person to another, the process often needs care and time. This might include discussing symptoms, reviewing family history, and choosing what testing is most helpful for the situation. Results then get explained in plain language, with attention to what they mean for everyday life.


At the same time, many people want to know what comes next. Kelan can help guide the conversation around options and follow-up care, so families feel less in the dark as they work through decisions.

Services & Conditions Treated

Bosma Arhinia Microphthalmia SyndromeChoanal AtresiaMicrophthalmiaFacioscapulohumeral Muscular Dystrophy (FSHD)

Publications

1 total

SMCHD1 has separable roles in chromatin architecture and gene silencing that could be targeted in disease.

Nature communications • May 10, 2021

Frequently Asked Questions

What conditions do you treat as a geneticist in Melbourne?
I specialise in genetic issues and offer insights for conditions like Bosma Arhinia Microphthalmia Syndrome, Choanal Atresia, Microphthalmia, and Facioscapulohumeral Muscular Dystrophy (FSHD).
What is Bosma Arhinia Microphthalmia Syndrome?
Bosma Arhinia Microphthalmia Syndrome is a rare genetic condition. If you’re dealing with this, you can discuss genetic factors and possible implications with me during a consultation.
What is Choanal Atresia?
Choanal Atresia is a congenital condition affecting the nasal passage. I can help explain genetic aspects and what it means for management and families.
What is Microphthalmia?
Microphthalmia refers to unusually small eyes. In a genetics context, we look at possible inherited factors and how they relate to your situation.
What is FSHD (Facioscapulohumeral Muscular Dystrophy)?
FSHD is a genetic muscle-wasting condition. I discuss genetic testing options and what results might mean for you or your family.
How do I book an appointment?
To book an appointment in Melbourne, please contact the clinic directly or use the booking system provided by the practice. I’ll guide you through what you’ll need for the visit.

Contact Information

Melbourne, VIC, Australia

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