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Home > Doctors > Dr Muhammed Shabeer

Dr Muhammed Shabeer

Dr Muhammed Shabeer

Consultant

Medical Genetics

  • BMH Kozhikode

  • BMH Kannur

Dr Muhammed Shabeer

Dr. Muhammed Shabeer is a highly proficient and dedicated Medical Geneticist committed to advancing patient care through precise genetic diagnosis and personalized management strategies. With strong clinical expertise, he specializes in Clinical Genetics for both pediatric and adult populations, addressing a wide spectrum of inherited and complex genetic conditions.

Dr. Muhammed Shabeer has particular expertise in Reproductive Genetics, Oncogenetics, and the evaluation and management of fetal infections, providing comprehensive guidance for patients and families. His approach integrates detailed clinical assessment with advanced Laboratory Genetics, including cytogenetics, molecular genetics, and biochemical analysis. This enables accurate diagnosis, risk assessment, and tailored treatment planning, ensuring high-quality, patient-centered care across diverse genetic disorders.

Phone - 7593812078 | WhatsApp - 9497826666 (Kannur)

OP Timings: Tuesday  09.00 AM -  04:00 PM

  • DrNB Medical Genetics - Sir Ganga Ram Hospital , National Board of Examination -  2023 - 2025
  • DNB Pediatrics - National Board of Examnination - 2020
  • MD Paediatrics - GMC Aurangabad , Maharashtra University of Health Sciences - 2017 - 2020
  • MBBS - Calicut Medical College , Kerala University of Health Sciences - 2010 - 2016
  • Consultant -  Medical Genetics -  Baby Memorial Hospital, Kannur - 2026 - Present
  • Specialist - Paediatrics - Nahas Alnas Hospital, Areekode - 2021 - 2023
  • Assistant Professor - GMC Aurangabad - 2020 - 2021
  • Clinical Genetics-Pediatric and Adult
  • Reproductive Genetics & Fetal infections
  • Oncogenetics
  • Laboratory Genetics-Cytogenetics, Molecular and Biochemical Genetics
  • 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

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