Beckwith-Wiedemann Syndrome (BWS) is a rare congenital disorder that causes abnormal growth in infants and children. It involves changes in genes on chromosome 11p15, affecting how cells divide and...
What is Pompe Disease?
Pompe disease, also referred to as Glycogen Storage Disease Type II (GSDII), is a rare genetic disorder characterized by muscle wasting...
Lennox Gastaut Syndrome is an epileptic disorder that occurs in infants and children. This condition is also called childhood encephalopathy. Infants or children with...
What is Kwashiorkar?
Kwashiorkor is a type of malnutrition linked with severe protein deficiency. It causes fluid retention, leading to a visibly distended and protruded...
Crigler Najjar syndrome is an inherited disorder in which genetic abnormality causes a poor function of enzymes involved in bilirubin processing, and it leads...
Avoidant/restrictive food intake disorder (ARFID) is among the common eating disorders in teenagers. A study suggestsNicely TA, Lane-Loney S, Masciulli E, Hollenbeak CS, Ornstein...
What is Congenital Rubella Syndrome?
Congenital Rubella Syndrome (CRS) is a viral disease resulting from primary maternal infection in newborns. It occurs when a...