Familial chondrocalcinosis, unspecified ankle and foot Save
ICD-10 code: M11.179
Disease category: M11.17: Familial chondrocalcinosis, ankle and foot
Familial Chondrocalcinosis: Understanding Ankle and Foot Involvement
Familial chondrocalcinosis is a rare genetic disorder characterized by the accumulation of calcium pyrophosphate crystals in the joints. While it can affect various joints in the body, this article focuses on its impact on the ankle and foot.
1. Ankle Involvement
In familial chondrocalcinosis, the ankle joint may experience inflammation and pain due to the deposition of calcium crystals. This can lead to stiffness, limited range of motion, and discomfort while walking or bearing weight on the affected ankle.
2. Foot Involvement
The foot is a complex structure consisting of numerous joints, and familial chondrocalcinosis can affect any of them. The most commonly involved joints include the midfoot, hindfoot, and the joints connecting the metatarsal bones to the phalanges.
3. Symptoms
Common symptoms of familial chondrocalcinosis in the ankle and foot may include:
- Pain and tenderness
- Swelling and redness
- Joint stiffness
- Decreased range of motion
- Difficulty walking or standing
4. Diagnosis
Diagnosing familial chondrocalcinosis in the ankle and foot involves a thorough medical history review, physical examination, and imaging tests. X-rays, ultrasound, or magnetic resonance imaging (MRI) can help visualize the presence of calcium crystal deposits and assess the extent of joint damage.
5. Treatment
Although we won't discuss treatment options in this article, it's important to note that managing familial chondrocalcinosis typically involves a combination of medication, lifestyle modifications, and, in some cases, surgical interventions. Consulting a healthcare professional is essential for accurate diagnosis and personalized treatment plans.
Conclusion:
Familial chondrocalcinosis can affect the ankle and foot, causing pain, inflammation, and restricted movement. Understanding the symptoms and seeking appropriate medical evaluation is crucial for early diagnosis and effective management of this rare genetic disorder.
Treatment of Familial chondrocalcinosis, unspecified ankle and foot:
Treatment Options for Familial Chondrocalcinosis, Unspecified Ankle and Foot
Familial Chondrocalcinosis, also known as calcium pyrophosphate deposition disease (CPPD), is a rare genetic condition that affects the joints, particularly the ankles and feet. This condition leads to the accumulation of calcium crystals in the cartilage, resulting in pain, inflammation, and difficulty mo...
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