Gastroenterologist, Internal Medicine Specialist, Hypertension Specialist, Consultant Physician, Diabetologist, General Physician, Hepatologist
MBBS, FCPS, ESBGH (UK), SCE Gastro (UK)
Gastroenterologist, Internal Medicine Specialist, Hypertension Specialist, Consultant Physician, Diabetologist, General Physician, Hepatologist
MBBS, FCPS, ESBGH (UK), SCE Gastro (UK)
Physiotherapist, Rehabilitation Specialist
DPT, Certified Women Health Practitioner (USA), Certified Exercise Physiologist (USA)
Physiotherapist, Rehabilitation Specialist
DPT, Certified Women Health Practitioner (USA), Certified Exercise Physiologist (USA)
Consultant Physician, Hepatologist, Gastroenterologist
MBBS, M.D Gastroenterology (Gold Medalist), FRCP (Gastroenterology & General Medicine)
Consultant Physician, Hepatologist, Gastroenterologist
MBBS, M.D Gastroenterology (Gold Medalist), FRCP (Gastroenterology & General Medicine)
Neonatologist, Pediatrician
MBBS, FCPS (Pediatric), FCPS (Neonatology)
Neonatologist, Pediatrician
MBBS, FCPS (Pediatric), FCPS (Neonatology)
Pediatrician, Asthma Specialist, Neonatologist
M.B.B.S, FRCPCH (UK), MRCPCH (Paeds), F.C.P.S (Paeds), PG Dip/MSc Allergy
Pediatrician, Asthma Specialist, Neonatologist
M.B.B.S, FRCPCH (UK), MRCPCH (Paeds), F.C.P.S (Paeds), PG Dip/MSc Allergy
Gastroenterologist, Hepatologist
MBBS, MCPS (Internal Medicine), FCPS (Gastroenterology & Hepatology), M.A.C.G (USA)
Gastroenterologist, Hepatologist
MBBS, MCPS (Internal Medicine), FCPS (Gastroenterology & Hepatology), M.A.C.G (USA)
General Physician, Family Physician, Internal Medicine Specialist, Consultant Physician, Diabetologist, Hepatologist
MBBS, FRACGP (Australia), Professional Certificate in Women Helath (Australia)
General Physician, Family Physician, Internal Medicine Specialist, Consultant Physician, Diabetologist, Hepatologist
MBBS, FRACGP (Australia), Professional Certificate in Women Helath (Australia)
Down syndrome (DS or DNS), also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21. It is typically associated with physical growth delays, characteristic facial features, and mild to moderate intellectual disability.