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Condition
Velopharyngeal Dysfunction (VPD)
Velopharyngeal dysfunction (VPD) is the inadequate separation of the oral and nasal cavities during speech and/or swallowing. At Nationwide Children’s Hospital, our experts in the Velopharyngeal Dysfunction Program provide specialized treatment for patients with speech disorders resulting from VPD.
Condition
Phimosis
Phimosis is a condition of the male foreskin where the skin is tight and unable to retract back behind the head of the penis. This condition is completely normal and physiologic in most baby boys whose penis is otherwise without abnormalities.
Condition
Clubfoot
In this Helping Hand™ document, we discuss clubfoot, a foot disorder in which the foot turns inward and downward at birth and remains in this position. In some cases, clubfoot can be corrected without surgery.
Tibial Stress Fracture
The tibia (shin bone) is the larger, and major weight bearing bone, of the two lower leg bones. A tibial stress fracture is a complete or incomplete break that develops over time, usually as a result of repeated activity.
Condition
Laryngomalacia
Laryngomalacia literally means “Soft Larynx”. It is caused by floppiness of the laryngeal tissues above the vocal cords (the supraglottic larynx).
Pulmonary Embolism
A pulmonary embolism is a blood clot that travels to the blood vessels in the lungs. You may hear a pulmonary embolism referred to as a “PE.”
Condition
Dysmenorrhea (Painful Menstruation)
A common reason patients experience painful menstruation, also known as dysmenorrhea, is because of inflammatory agents, called prostaglandins, which are released from the lining of the uterus during menstruation.
Condition
Tetralogy of Fallot (TOF)
Tetralogy of Fallot is a congenital heart defect that is made up of 4 problems and results in not enough blood flow to the lungs.
Condition
Pulmonary Atresia
Pulmonary atresia is a heart defect in children that affects blood flow to the lungs. It can be treated with surgery or catheterization
Condition
Rett Syndrome
Rett syndrome affects the way the brain develops. This rare condition causes children to lose language and motor skills starting around age 6 to 18 months.