Leptin Deficiency, also known as Congenital leptin deficiency (CLD), is a rare inherited disorder that causes early-onset obesity (in infants). Patients are born with normal weight, but they become...
Cradle cap, also known as infantile seborrheic dermatitis, is a chronic, common skin condition in newborn babies characterized by greasy, yellow patches on the...
Batten disease is a rare disease affecting the nervous system. Weak eyesight, seizures, slowed growth rate, delays in cognitive learning, motor skills disability, and...
Pyloric stenosis is a disease in infants that develops when the pylorus muscle of their stomach becomes abnormally thick. The thickness of the pylorus...
What is Thrush?
Thrush in babies, also known as oral thrush or oropharyngeal candidiasis, is a common fungal infection caused by an overgrowth of Candida...
What is Prader-Willi Syndrome?
Prader-Willi syndrome (PWS) is a rare multisystem genetic disorder affecting the metabolic, endocrine, and neurologic systems due to abnormalities on chromosome...
Omphalocele is an inborn disorder in which a defect in your child's central abdominal wall causes protrusion of the abdominal contents or organs outside...