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Jaundice is a common condition that affects 60-80% of newborns in the United States. It occurs when there is a buildup of bilirubin, a yellow…
Fibrodysplasia Ossificans Progressiva (FOP) is a rare genetic condition that causes the body's soft tissues, such as muscles, ligaments, and tendons,…
Treacher Collins Syndrome (TCS) is a rare genetic condition that affects the development of a baby's face. If your child has been diagnosed with TCS,…
Spinal muscular atrophy (SMA) is a genetic disorder that primarily affects babies and children, but can also develop in adults later in life, causing…
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Get a free consultationNewborn jaundice is a common condition that causes a baby's skin and eyes to look yellow. It affects about 60% of full-term babies and 80% of…
Cystic fibrosis (CF) is a genetic disorder that affects multiple organs in the body, primarily the lungs and pancreas. People with CF inherit a…
Ventricular septal defect (VSD) is a common congenital heart defect that occurs in infants. It is characterized by a hole in the wall (septum)…
Mucopolysaccharidosis Type I, or MPS I, is a rare genetic disorder that affects children. It is caused by a deficiency in an enzyme called alpha-L…
Pfeiffer syndrome is a rare genetic disorder that affects the development of a baby's skull and face. This condition causes the skull bones to fuse…
Infantile spasms, also known as West syndrome, is a rare type of seizure disorder that affects babies. If your baby has been diagnosed with infantile…
Klinefelter syndrome is a genetic condition that affects males who are born with an extra X chromosome. Instead of the typical XY chromosome pattern,…
Congenital hydrocephalus is a condition present at birth where an excessive amount of cerebrospinal fluid (CSF) accumulates in the brain. CSF is a…
Muscular dystrophy is a group of genetic disorders that cause progressive muscle weakness and loss of muscle mass. While there are many types of…
