Thomson disease is a rare, inherited disorder impacting various parts of the body. It is also known as Rothmund-Thomson Syndrome (RTS).
Understanding Rothmund-Thomson Syndrome (RTS)
Rothmund-Thomson Syndrome (RTS) is characterized by affecting multiple areas, including:
- Skin: A distinctive red, blistering rash typically appears on the face in early infancy.
- Eyes: Can cause cataracts.
- Bones: Skeletal abnormalities may be present.
- Hair: Sparse hair.
- Teeth: Dental anomalies can occur.
Key Features of Thomson Disease (RTS)
| Feature | Description |
|---|---|
| Inheritance | Inherited |
| Skin Manifestations | Red, blistering rash on the face, appearing in early infancy. |
| Other Symptoms | Eye problems, bone abnormalities, sparse hair, and dental anomalies. |
