Omphalocele: Causes, Treatment & Support
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...
Zellweger Syndrome: Shedding Light on the Rare Genetic Disorder
What is Zellweger Syndrome?
Zellweger syndrome is a rare genetic disorder that disrupts cellular function and usually appears soon after birth. Named after Dr. Hans...
Congenital Syphilis: Diagnoses, Symptoms, Treatment
Syphilis results from infection with Treponema Pallidum. Congenital Syphilis (CS) occurs when the Treponema bacterium is transmitted from the mother to the fetus (unborn...
Anencephaly: Exploring a Rare Neural Tube Defect
Anencephaly is a serious but rare birth defect. Babies with this birth defect are born without some portions of the brain and skull. The...
Pierre Robin Syndrome: Understanding the Condition
Pierre Robin Syndrome, a rare congenital disorder, manifests with facial and mouth deformities that impede breathing. It can occur independently or alongside syndromes like...
Pompe Disease: Understanding Symptoms & Treatments
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...
