Pediatrician, Neonatologist
MBBS, FCPS (Pediatrics), MRCPCH (England), ICT (Neonatology), OGT (Pulmonology)
Pediatrician, Neonatologist
MBBS, FCPS (Pediatrics), MRCPCH (England), ICT (Neonatology), OGT (Pulmonology)
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)
Rehabilitation Specialist, Speech and Language Pathologist, Psychologist, Counselor
PhD (Special Education), Post Doctorate PhD (UK)
Rehabilitation Specialist, Speech and Language Pathologist, Psychologist, Counselor
PhD (Special Education), Post Doctorate PhD (UK)
Gastroenterologist, Hypertension Specialist, Hepatologist
MBBS, FCPS (Gastroenterology), European Speciality Certificate in Gastroenterology and Hepatalogy (UK)
Gastroenterologist, Hypertension Specialist, Hepatologist
MBBS, FCPS (Gastroenterology), European Speciality Certificate in Gastroenterology and Hepatalogy (UK)
Gastroenterologist, Internal Medicine Specialist, Hypertension Specialist, Consultant Physician, Diabetologist, Hepatologist
MBBS, FCPS (Gastroenterology), SCE Gastroenterology (UK), ESB Gastroenterology (EU)
Gastroenterologist, Internal Medicine Specialist, Hypertension Specialist, Consultant Physician, Diabetologist, Hepatologist
MBBS, FCPS (Gastroenterology), SCE Gastroenterology (UK), ESB Gastroenterology (EU)
Consultant Physician, Hepatologist, Gastroenterologist
M.B.B.S., M.D Gastroenterology (Gold Medalist), FRCP (Gastroenterology & General Medicine)
Consultant Physician, Hepatologist, Gastroenterologist
M.B.B.S., M.D Gastroenterology (Gold Medalist), FRCP (Gastroenterology & General Medicine)
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.