TAN syndrome: Difference between revisions
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Revision as of 01:29, 18 March 2025
TAN Syndrome is a rare medical condition characterized by Thrombocytopenia, Absent radius, and Neutropenia. It is a genetic disorder that affects the development of certain body parts.
Symptoms
The main symptoms of TAN Syndrome include:
- Thrombocytopenia: This is a condition characterized by low levels of platelets in the blood. Platelets are necessary for blood clotting, and a deficiency can lead to easy bruising and excessive bleeding.
- Absent radius: This refers to the absence of the radius bone in the forearm. This can result in a variety of physical abnormalities, including a shortened arm and limited mobility of the hand.
- Neutropenia: This is a condition characterized by a low number of neutrophils, a type of white blood cell that fights infection. This can result in an increased susceptibility to infections.
Causes
TAN Syndrome is a genetic disorder, which means it is caused by abnormalities in a person's genes. It is inherited in an autosomal recessive manner, which means both parents must carry a copy of the mutated gene for a child to be affected.
Diagnosis
The diagnosis of TAN Syndrome is typically made based on the presence of the characteristic symptoms. Genetic testing can confirm the diagnosis.
Treatment
There is currently no cure for TAN Syndrome. Treatment is aimed at managing the symptoms and may include blood transfusions for thrombocytopenia, antibiotics for infections due to neutropenia, and physical therapy or surgery for abnormalities related to the absent radius.
See Also
References
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