Family mapping of previously identified patients with pathogenic or likely pathogenic ALPL variants using predictive genotyping and detailed phenotyping approach: the FAME case-control study.
Journal: JBMR plus
Year: December 27, 2024
Clinical Geneticist
5
Meena Balasubramanian
Adelaide
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Services Offered by Meena Balasubramanian
Osteogenesis Imperfecta
Carpenter Syndrome
Hydrocephalus Skeletal Anomalies
Aarskog Syndrome
Angelman Syndrome
Early Infantile Epileptic Encephalopathy
Hydranencephaly
Hypotonia
Juvenile Primary Osteoporosis
Lethal Congenital Contracture Syndrome
Recessive Chondrodysplasia Punctata 1
Absence Seizure
Achalasia Microcephaly Syndrome
Achondrogenesis
Acromesomelic Dysplasia
Acromesomelic Dysplasia Campailla Martinelli Type
Acromesomelic Dysplasia Hunter Thompson Type
Acromesomelic Dysplasia Maroteaux Type
Acute Pain
Alternating Hemiplegia of Childhood
Arterial Tortuosity Syndrome
Arthrogryposis Multiplex Congenita
Autism Spectrum Disorder
Brachydactyly Mononen Type
Chondrodysplasia Punctata Syndrome
Chondrodystrophy
Chromosome 7q Duplication
Congenital Contractures
Congenital Hypothyroidism
Congenital Radioulnar Synostosis
Cornelia De Lange Syndrome
Corpus Callosum Agenesis
Cortical Dysplasia
Craniosynostosis
Crouzon Syndrome
Cutis Laxa
Dandy-Walker Syndrome
Ehlers-Danlos Syndrome (EDS)
Epilepsy
Epilepsy in Children
Focal or Multifocal Malformations in Neuronal Migration
Fractured Spine
Generalized Tonic-Clonic Seizure
Hemiplegia
Holoprosencephaly
Hydrocephalus
Hypophosphatasia (HPP)
Increased Head Circumference
Joubert Syndrome
KBG Syndrome
Metopic Ridge
Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1)
Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2)
Microcephaly
Mosaicism
Movement Disorders
Myoglobinuria Recurrent
Neonatal Hypothyroidism
Osteoporosis
Plagiocephaly
Primary Lateral Sclerosis
Rhabdomyolysis
Russell-Silver Dwarfism
Schwartz-Jampel Syndrome
Seizures
Tracheobronchomalacia
Vascular Ehlers-Danlos Syndrome (VEDS)
West Syndrome
X-Linked Chondrodysplasia Punctata 2
X-Linked Spondyloepiphyseal Dysplasia Tarda
About Of Meena Balasubramanian
Meena Balasubramanian is a female medical professional who helps patients with a variety of health conditions like bone disorders, brain issues, genetic syndromes, and developmental delays. She specializes in treating rare and complex diseases that affect the skeletal system, brain, and overall development of children and adults.
Meena uses her special skills and knowledge to diagnose and treat conditions such as osteoporosis, epilepsy, autism, and genetic disorders. She is known for her expertise in managing conditions like hydrocephalus, skeletal anomalies, and movement disorders.
Patients trust Meena because she communicates with them in a caring and compassionate way. She listens to their concerns, explains treatments clearly, and involves them in decision-making about their care. Her patients appreciate her dedication to providing the best possible outcomes for their health.
To stay updated with the latest medical knowledge and research, Meena regularly attends conferences, reads scientific journals, and collaborates with other medical experts. She is committed to lifelong learning and continuously seeks to improve her skills and expertise.
Meena works closely with her colleagues and values teamwork in providing comprehensive care to patients. She collaborates with other medical professionals to ensure that patients receive holistic and coordinated treatment plans. Her approach to working with others is respectful, collaborative, and patient-centered.
Meena's work has positively impacted many patients' lives by improving their health outcomes, quality of life, and overall well-being. Her dedication to providing excellent care and her commitment to advancing medical knowledge have made a significant difference in the lives of those she treats.
One of Meena's notable publications is the "Family mapping of previously identified patients with pathogenic or likely pathogenic ALPL variants using predictive genotyping and detailed phenotyping approach: the FAME case-control study" published in JBMR plus. This study highlights her contribution to advancing genetic research and personalized medicine for patients with specific bone disorders.
Meena Balasubramanian's expertise, compassion, and dedication to her patients have made her a trusted and respected medical professional in her field.
Publications by Meena Balasubramanian
Patient Reviews for Meena Balasubramanian
Liam O'Malley
Meena Balasubramanian is an amazing Clinical Geneticist. She explained everything in a way that was easy for me to understand. Highly recommend her!
Isla Patel
Dr. Balasubramanian is a fantastic Clinical Geneticist. She was very kind and patient with me during my consultation. I felt very comfortable discussing my concerns with her.
Cooper Nguyen
Meena Balasubramanian is a top-notch Clinical Geneticist. She was thorough in her assessment and provided me with valuable insights into my genetic condition. I am grateful for her expertise.
Sienna Wong
I had a great experience with Dr. Balasubramanian, who is a skilled Clinical Geneticist. She was compassionate and knowledgeable, making me feel at ease throughout the appointment.
Elijah Kaur
Meena Balasubramanian is an exceptional Clinical Geneticist. She took the time to listen to my concerns and provided me with personalized care. I highly recommend her to anyone seeking genetic counseling.
Harper Das
Dr. Balasubramanian is a wonderful Clinical Geneticist. She was very thorough in her explanations and made sure I understood everything clearly. I left the appointment feeling informed and supported.
Ava Raj
Meena Balasubramanian is a brilliant Clinical Geneticist. She was very patient and answered all my questions with clarity. I felt confident in her expertise and guidance.
Mason Singh
I had a positive experience with Dr. Balasubramanian, who is an excellent Clinical Geneticist. She was attentive and caring, providing me with valuable information about my genetic condition.
Frequently Asked Questions About Meena Balasubramanian
What conditions does Meena Balasubramanian specialize in as a Clinical Geneticist?
Meena Balasubramanian specializes in diagnosing and managing genetic conditions such as undefined, undefined, and undefined.
How can Meena Balasubramanian help individuals with a family history of genetic disorders?
Meena Balasubramanian can provide genetic counseling and testing to assess the risk of inherited conditions and offer guidance on management and prevention strategies.
What is the process for genetic testing with Meena Balasubramanian?
The process typically involves a consultation to discuss the individual's medical history and family background, followed by genetic testing if deemed necessary. Results are then interpreted and explained to the patient.
Can Meena Balasubramanian provide prenatal genetic counseling and testing?
Yes, Meena Balasubramanian offers prenatal genetic counseling to expectant parents to assess the risk of genetic conditions in the baby and can arrange for prenatal genetic testing if required.
How does Meena Balasubramanian stay updated on the latest advancements in clinical genetics?
Meena Balasubramanian regularly attends conferences, workshops, and engages in continuing education to stay abreast of the latest research and advancements in the field of clinical genetics.
What should patients expect during a consultation with Meena Balasubramanian?
During a consultation, patients can expect a comprehensive review of their medical and family history, discussion of any concerns or symptoms, genetic testing recommendations if needed, and personalized counseling on managing genetic conditions.
