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Pediatric Geneticist

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Thuong T. Ha

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Adelaide

Quick Appointment for Thuong T. Ha

No OPD information available

Services Offered by Thuong T. Ha

  • Aicardi Syndrome

  • Familial Porencephaly

  • Porencephaly

  • Seckel Syndrome

  • Acromicric Dysplasia

  • Autosomal Recessive Primary Microcephaly

  • Brachydactyly Mononen Type

  • Caffey Disease

  • Chondrodystrophy

  • Cortical Dysplasia

  • Encephalocele

  • Knobloch Syndrome

  • Lennox-Gastaut Syndrome (LGS)

  • Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1)

  • Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2)

  • Periventricular Heterotopia

  • Polymicrogyria

  • Rhabdomyolysis

  • RUNX1 Familial Platelet Disorder

  • Schwartz-Jampel Syndrome

  • X-Linked Spondyloepiphyseal Dysplasia Tarda

About Of Thuong T. Ha

Thuong T. Ha helps kids with special health conditions like Aicardi Syndrome, Porencephaly, Seckel Syndrome, and more. They are experts in treating rare disorders that affect the brain, bones, and muscles.

Thuong T. Ha uses special skills and treatments to help their patients feel better. They are good at understanding complex medical problems and finding ways to improve their patients' health.

Patients trust Thuong T. Ha because they are kind, caring, and always listen to their concerns. They explain things in a simple way so patients can understand what's happening with their health.

Thuong T. Ha stays updated with the latest medical knowledge by reading research papers and attending conferences. This helps them provide the best care for their patients.

Thuong T. Ha works well with other medical professionals to make sure patients get the best treatment possible. They share knowledge and collaborate with colleagues to find solutions for complex cases.

Thuong T. Ha's work has helped many kids live healthier lives. By diagnosing rare disorders and providing specialized care, they have made a positive impact on their patients and their families.

One of Thuong T. Ha's notable publications is about assessing the clinical validity of gene-disease relationships. This shows their commitment to advancing medical knowledge and improving patient care.

In summary, Thuong T. Ha is a dedicated medical professional who specializes in treating rare disorders and making a difference in the lives of their patients.

Publications by Thuong T. Ha

Frequently Asked Questions About Thuong T. Ha

What conditions do Pediatric Geneticists like Thuong T. Ha typically diagnose and treat?

Pediatric Geneticists like Thuong T. Ha specialize in diagnosing and treating genetic disorders and conditions that are present from birth or develop during childhood.

How can Thuong T. Ha help families with a history of genetic disorders?

Thuong T. Ha can provide genetic counseling and testing to families with a history of genetic disorders to assess the risk of passing on genetic conditions to their children and offer guidance on family planning.

What should I expect during a consultation with Thuong T. Ha?

During a consultation with Thuong T. Ha, you can expect a comprehensive evaluation of your child's medical history, a physical examination, genetic testing if needed, and personalized treatment recommendations.

What are the benefits of genetic testing for children?

Genetic testing can help identify the underlying cause of a child's health issues, guide treatment decisions, provide information on prognosis, and offer valuable insights for families about their child's condition.

How can Thuong T. Ha assist in managing rare genetic disorders in children?

Thuong T. Ha can collaborate with a multidisciplinary team to develop a personalized treatment plan for children with rare genetic disorders, including coordinating care with other specialists and providing ongoing support to families.

What resources does Thuong T. Ha offer to support families of children with genetic conditions?

Thuong T. Ha can connect families with support groups, educational materials, and community resources to help them navigate the challenges of raising a child with a genetic condition and access the necessary support services.
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