Cystic Fibrosis

Cystic fibrosis (CF) is a hereditary and progressive genetic disorder that primarily affects the respiratory and digestive systems. This life-limiting condition results from a faulty gene that affects the production of a protein responsible for regulating salt and water movement in the body’s cells.

Galactosemia

Galactosemia is a rare and inherited metabolic disorder that affects the body’s ability to break down galactose, a sugar found in milk and other dairy products. It occurs when there is a deficiency of certain enzymes needed to convert galactose into glucose, resulting in the accumulation of toxic substances in the body.

Gastroenteritis

Gastroenteritis, commonly known as the stomach flu, is a prevalent and often self-limiting gastrointestinal infection that is characterized by inflammation of the stomach and intestines, leading to symptoms such as nausea, vomiting, diarrhea, and abdominal cramps.

Gastroesophageal Reflux

Gastroesophageal reflux (GER) is a common and often benign condition that affects people of all ages. It occurs when stomach contents, including acid and digestive enzymes, flow backward into the esophagus, causing symptoms like heartburn and regurgitation.

Hemophilia

Hemophilia results from mutations at the factor VIII or IX loci on the X chromosome and each occurs in mild, moderate, and severe forms.

Hydrocephalus

Hydrocephalus is a condition characterized by an excess of cerebrospinal fluid (CSF) within the ventricular and subarachnoid spaces of the cranial cavity.

Imperforate Anus

Imperforate anus is a congenital abnormality that occurs when the opening of the anus is either absent or improperly formed in newborns. This condition can range from a partial obstruction to a complete absence of the anal opening, leading to difficulties in passing stool.