Dr. Muhammed Shabeer P

Consultant – Clinical Genetics & Paediatric Genetics

MBBS, MD (Paediatrics), DNB (Paediatrics), DrNB (Medical Genetics)

Dr. Muhammed Shabeer P is a highly qualified Clinical Geneticist and Paediatrician with expertise in the diagnosis, evaluation, and management of inherited genetic and metabolic disorders in children and adults. He completed his MBBS from Calicut Medical College (Kerala University of Health Sciences), followed by MD Paediatrics from GMC Aurangabad and DNB Paediatrics from the National Board of Examinations. He further pursued DrNB in Medical Genetics from the prestigious Sir Ganga Ram Hospital, New Delhi.

With a strong foundation in paediatrics and advanced training in clinical genetics, Dr. Shabeer has extensive experience in diagnosing rare genetic disorders, inborn errors of metabolism, neurogenetic disorders, dysmorphic syndromes, developmental delays, and congenital anomalies. His areas of expertise also include reproductive genetics, fetal genetics, oncogenetics, and laboratory genetics, offering comprehensive genetic evaluation and counselling for individuals and families.

Prior to joining Almas Hospital, he served as Assistant Professor in the Department of Paediatrics at GMC Aurangabad and later worked as a Specialist Paediatrician at Nahas Almas Hospital, Areekode, where he gained valuable clinical and academic experience.

Dr. Shabeer has made significant academic contributions through research publications in leading national and international peer-reviewed journals, particularly in the fields of clinical genetics, metabolic disorders, neurogenetics, and rare genetic diseases. His research reflects a commitment to advancing precision medicine and improving outcomes through early diagnosis and evidence-based genetic care.

At Almas Hospital, Dr. Muhammed Shabeer is dedicated to delivering comprehensive, compassionate, and patient-centred genetic services, integrating the latest advances in genomic medicine to provide accurate diagnosis, personalized treatment strategies, and informed genetic counselling for patients and their families

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