Laura J. Sharpe is a Clinical Geneticist based in Chancellery Walk, Kensington, NSW 2033, Australia. In her work, she helps people when there’s a concern about a genetic condition, and it can feel a bit confusing and stressful at times. Genetics can explain why symptoms show up in a child, why health issues run in families, or why things don’t quite match what doctors expected.
Laura focuses on several rare genetic syndromes and related conditions. This includes Smith-Lemli-Opitz Syndrome, where people may have growth and development differences, and where cholesterol and other body functions can be affected. She also supports families dealing with Cat Eye Syndrome, a condition that can cause differences in body development, and often involves the eyes and other parts of the body.
Another area she looks after is Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limbs Defects. This can involve one side of the body more than the other, with skin changes and limb differences. At times, families notice these signs early on, and want clear answers about what’s going on and what it could mean for the future.
Laura also works with people affected by Cri-Du-Chat Syndrome. This name comes from the sound some babies may make, and the condition can bring learning and developmental challenges, along with other health needs that may vary from person to person. Because no two cases are exactly the same, it helps when care is steady and plain-speaking.
Skin-related genetic conditions are also part of her practice, including Erythroderma and Exfoliative Dermatitis. These can involve widespread redness, irritation, and peeling of the skin. In many cases, families are trying to manage symptoms day to day, and they want help understanding the cause and the options that might make life easier.
Over time, genetic conditions like these can affect more than one part of health. They may involve development, growth, skin care, and long-term monitoring. Laura’s role is to bring the genetic pieces together in a way that makes sense for the person and their family, using the clinical information available to guide next steps.