Pediatrician, Neonatologist
M.B.B.S., M.C.P.S, F.C.P.S (Pediatric), RSC (USA), PGPN , M.H.P.E
Pediatrician, Neonatologist
M.B.B.S., M.C.P.S, F.C.P.S (Pediatric), RSC (USA), PGPN , M.H.P.E
Gastroenterologist, Hepatologist
MBBS, FMGEMS, FLEX, F.A.C.P, Diplomate of the American Board of Internal Medicine, Diplomate of the American Board of Gastroenterology
Gastroenterologist, Hepatologist
MBBS, FMGEMS, FLEX, F.A.C.P, Diplomate of the American Board of Internal Medicine, Diplomate of the American Board of Gastroenterology
Rehab Medicine, Rehabilitation Specialist
M.B.B.S., F.C.P.S.,M.D, F.A.A.P.M (USA), Diplomate American Board of Physical Medicine & Rehabilitation
Rehab Medicine, Rehabilitation Specialist
M.B.B.S., F.C.P.S.,M.D, F.A.A.P.M (USA), Diplomate American Board of Physical Medicine & Rehabilitation
Pediatrician, Pediatric Rheumatologist
MBBS, DCH, FCPS (Pediatrics), PGPN (Boston), EULAR online course in Pediatric Rheumatology, EULAR online course for Systemic Lupus Erythematosus, EULAR online course of Systemic Sclerosis
Pediatrician, Pediatric Rheumatologist
MBBS, DCH, FCPS (Pediatrics), PGPN (Boston), EULAR online course in Pediatric Rheumatology, EULAR online course for Systemic Lupus Erythematosus, EULAR online course of Systemic Sclerosis
Hepatologist, Gastroenterologist
M.B.B.S, F.C.P.S (Gastroenterology)
Hepatologist, Gastroenterologist
M.B.B.S, F.C.P.S (Gastroenterology)
Gastroenterologist, Hepatologist
MBBS, MRCP (UK), FCPS (Gastroenterology), M.D (USA), Gastroenterology SCE (UK) , European Board of Gastroenterology and Hepatology (EBGH)
Gastroenterologist, Hepatologist
MBBS, MRCP (UK), FCPS (Gastroenterology), M.D (USA), Gastroenterology SCE (UK) , European Board of Gastroenterology and Hepatology (EBGH)
Pediatric Gastroenterologist, Pediatrician
M.B.B.S., F.C.P.S (Pediatrics), F.C.P.S (Pediatric Gastroenterology)
Pediatric Gastroenterologist, Pediatrician
M.B.B.S., F.C.P.S (Pediatrics), F.C.P.S (Pediatric Gastroenterology)
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.