Emergency
Dr. Muhammed Shabeer P

Dr. Muhammed Shabeer P

Junior Consultant – Advanced Medical Genetics

Meitra Hospital

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About

Dr. Muhammed Shabeer is a Medical Geneticist with specialized training in the diagnosis, evaluation, and management of genetic disorders across all age groups. He combines clinical expertise with advanced genetic testing methodologies to provide accurate diagnoses, individualized care plans, and informed genetic counseling for patients and their families.

With a strong background in pediatrics and medical genetics, Dr. Shabeer focuses on identifying the underlying genetic causes of complex medical conditions and translating genetic findings into practical clinical recommendations. His approach emphasizes evidence-based medicine, multidisciplinary collaboration, and patient-centered care.

Dr. Shabeer has extensive experience in both clinical and laboratory genetics, enabling him to integrate detailed patient assessments with modern diagnostic technologies, including cytogenetic, molecular, and biochemical testing. His goal is to support patients and families through every stage of the diagnostic and management process while promoting informed healthcare decisions.

Qualification

  • MBBS
  • MD in Pediatrics
  • DNB in Pediatrics
  • DrNB in Medical Genetics  

Expertise/Interest Area

  • Clinical Genetics
  • Pediatric and Adult Genetic Medicine
  • Reproductive Genetics
  • Fetal Infections and Prenatal Evaluation
  • Cancer Genetics (Oncogenetics)

Research and Publications

  • Role of Vitamin E supplementation in treatment resistant epilepsy in children in the age group of 1-12 years.- European Journal of Molecular & Clinical Medicine
  • Using multiple modalities to confirm diagnosis in patients with suspected peroxisome biogenesis disorders - Molecular Genetics and Metabolism
  • KIF11-related Microcephaly with Chorioretinopathy and Pachygyria: A Case Report of a Denovo Start Codon Variant in an Indian Child - Genetic Clinics
  • Unmasking Genetic Mechanisms for Homocystinuria due to MethylenetetrahydrofolateReductase Deficiency - Genetic Clinics
  • Transient Infantile Liver Failure due to TRMU Deficiency: The Role of Rapid Exome Sequencing - Indian Journal of Pediatrics