Dr. Vinu N – Medical Geneticist in Bangalore

Dr. Vinu N is an experienced Consultant Medical Geneticist specializing in Pediatric and Adult Medical Genetics at Rainbow Children's Hospital, Marathahalli, Bengaluru.

With 10+ years of experience, Dr. Vinu N specializes in the diagnosis, management and genetic counselling of children, adults and families affected by genetic, metabolic and inherited disorders.

She completed her MD in Pediatrics from B. J. Government Medical College, Pune, followed by three years of super-specialty training in Medical Genetics (DNB-SS) from Sir Ganga Ram Hospital, New Delhi.

Dr. Vinu N is the recipient of the President Gold Medal for DNB-SS in Medical Genetics. She has also received awards for paper presentations at national and international conferences.

Her clinical expertise includes the evaluation and management of genetic disorders, dysmorphic syndromes, skeletal dysplasias, neuromuscular disorders, metabolic disorders, autism, congenital malformations, intellectual disability, deafness, albinism, thalassemia, short stature and haemophilia.

She also provides pre-conception and prenatal genetic counselling for families with a history or risk of genetic disorders. Her expertise includes assessment of pregnancies affected by aneuploidy risk, teratogen exposure, intrauterine infections and fetal ultrasound abnormalities.

Her approach focuses on accurate diagnosis, personalized genetic counselling and coordinated management to help patients and families understand inherited conditions and available care options.

Dr. Vinu N also evaluates families with a history of recurrent pregnancy loss, unexplained stillbirths, neonatal deaths and inherited conditions, helping families understand genetic risks and appropriate testing options.

Dr. Vinu N's Medical Genetics Treatments & Services

Dr. Vinu N provides specialized genetic evaluation, diagnosis and counselling for children, adults and families with suspected or confirmed inherited and metabolic conditions.

Genetic Disorder Diagnosis

Comprehensive evaluation of children and adults with suspected inherited or genetic disorders.

Genetic Counselling

Individualized counselling to help patients and families understand genetic conditions, inheritance patterns, testing and recurrence risks.

Dysmorphic Syndrome Evaluation

Clinical assessment of children with unusual facial features, congenital abnormalities or other features suggestive of a genetic syndrome.

Skeletal Dysplasia Evaluation

Evaluation of children with suspected inherited skeletal and bone growth disorders.

Neuromuscular Disorder Evaluation

Genetic assessment of children and families affected by suspected inherited neuromuscular disorders.

Metabolic Disorder Evaluation

Assessment of suspected inherited metabolic disorders and related clinical conditions.

Autism Genetic Evaluation

Genetic assessment for selected children with autism and associated developmental or syndromic features.

Intellectual Disability Evaluation

Evaluation of children with intellectual disability to identify possible underlying genetic causes.

Short Stature Evaluation

Assessment of children with unexplained short stature or suspected genetic growth disorders.

Pre-Conception Genetic Counselling

Genetic counselling for couples who have a personal or family history of inherited disorders or concerns about genetic risks.

Prenatal Genetic Counselling

Counselling and evaluation for pregnancies with suspected genetic or chromosomal abnormalities.

Recurrent Pregnancy Loss Evaluation

Genetic assessment and counselling for families experiencing recurrent pregnancy loss or unexplained pregnancy complications.

Fetal Ultrasound Abnormality Evaluation

Genetic evaluation and counselling when fetal ultrasound identifies structural or developmental abnormalities.

Familial Cancer Risk Assessment

Genetic assessment for families with a history suggestive of inherited cancer predisposition.