Odonto–tricho–ungual–digital–palmar syndrome
Odonto–tricho–ungual–digital–palmar syndrome is a rare genetic disorder characterized by dental, hair, nail, and digital abnormalities, as well as palmar hyperkeratosis. The syndrome is extremely rare, with only a few reported cases worldwide.
Symptoms and Signs[edit | edit source]
The symptoms of Odonto–tricho–ungual–digital–palmar syndrome can vary greatly from person to person. However, common symptoms include:
- Dental abnormalities such as missing or malformed teeth
- Hair abnormalities including sparse or absent hair
- Nail abnormalities such as ridged or absent nails
- Digital abnormalities including fused or missing fingers or toes
- Palmar hyperkeratosis, a condition characterized by thickened skin on the palms of the hands
Causes[edit | edit source]
The exact cause of Odonto–tricho–ungual–digital–palmar syndrome is currently unknown. However, it is believed to be a genetic disorder, passed down through families.
Diagnosis[edit | edit source]
Diagnosis of Odonto–tricho–ungual–digital–palmar syndrome is typically made based on the presence of the characteristic physical findings. Genetic testing may also be used to confirm the diagnosis.
Treatment[edit | edit source]
There is currently no cure for Odonto–tricho–ungual–digital–palmar syndrome. Treatment is typically focused on managing the symptoms and improving the quality of life for those affected. This may include dental care, dermatological treatments, and physical therapy.
See Also[edit | edit source]
- Genetic disorders
- Dental abnormalities
- Hair abnormalities
- Nail abnormalities
- Digital abnormalities
- Palmar hyperkeratosis
References[edit | edit source]
External Links[edit | edit source]
Odonto–tricho–ungual–digital–palmar syndrome Resources | |
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Contributors: Prab R. Tumpati, MD