trichorhinophalangeal syndrome type II

Langer-Giedon syndrome, also known as trichorhinophalangeal syndrome type 2, is a very rare, genetic, multiple congenital anomaly disorder characterized by bone abnormalities, distinctive facial features, multiple exostoses, and intellectual disability.

What is trichorhinophalangeal syndrome type II?

trichorhinophalangeal syndrome type II is a medical condition. A condition is a disease, disorder, or abnormal state that affects the body or mind. This page provides educational information only and is not a diagnosis.

If you think you may have trichorhinophalangeal syndrome type II, speak with a qualified healthcare provider for evaluation and guidance.

Symptoms that may be associated with trichorhinophalangeal syndrome type II

Alopecia of scalpArthralgiaDeeply set eyeDry skinFebrile convulsionGastroesophageal refluxHearing impairmentHemiparesisScapular wingingSeizureVomiting

When to seek medical care

Seek medical advice if you have symptoms that are severe, persistent, or affecting your daily life. Emergency care is needed for symptoms like chest pain, difficulty breathing, confusion, or severe weakness.