Familial chondrocalcinosis, unspecified shoulder digital illustration

Familial chondrocalcinosis, unspecified shoulder Save


ICD-10 code: M11.119

Disease category: M11.11: Familial chondrocalcinosis, shoulder

Familial Chondrocalcinosis: Unspecified Shoulder

Familial chondrocalcinosis is a rare genetic disorder characterized by the accumulation of calcium pyrophosphate crystals in the joints. Although it can affect various joints in the body, this article focuses on familial chondrocalcinosis in the shoulder.

1. Symptoms:

  1. Joint pain: Individuals with familial chondrocalcinosis may experience pain in their shoulders, which can range from mild discomfort to severe pain.
  2. Swelling: Swelling around the affected shoulder joint can occur due to inflammation caused by the crystal deposits.
  3. Restricted movement: The buildup of calcium pyrophosphate crystals can limit the range of motion in the shoulder, making it difficult to perform certain movements.

2. Causes:

Familial chondrocalcinosis is primarily caused by genetic mutations that affect the production and breakdown of calcium pyrophosphate crystals. These mutations can be inherited from one or both parents.

3. Diagnosis:

Diagnosing familial chondrocalcinosis in the shoulder involves a combination of medical history assessment, physical examination, and imaging tests. X-rays and ultrasound scans can help visualize the calcium deposits and assess the extent of joint damage.

4. Risk factors:

Although familial chondrocalcinosis is primarily a genetic condition, certain factors can increase the risk of developing the disorder. These include advancing age, obesity, and previous joint injuries.

5. Management:

Currently, there is no specific treatment for familial chondrocalcinosis; however, management focuses on relieving symptoms and preventing complications. Options may include pain management, physical therapy, and lifestyle modifications such as weight loss and joint protection strategies.

6. Outlook:

Familial chondrocalcinosis is a lifelong condition, and the severity of symptoms may vary from person to person. With appropriate management, individuals with familial chondrocalcinosis can lead active lives and minimize the impact on their shoulder joint function.

In conclusion, familial chondrocalcinosis affecting the shoulder joint can cause pain, swelling, and restricted movement. While there is currently no cure, proper management can help alleviate symptoms and improve quality of life for individuals with this condition.

Treatment of Familial chondrocalcinosis, unspecified shoulder:

Treatment Options for Familial Chondrocalcinosis, Unspecified Shoulder

Familial chondrocalcinosis is a rare genetic disorder characterized by the accumulation of calcium pyrophosphate dihydrate crystals in the joints. When this condition affects the shoulder, it is known as familial chondrocalcinosis, unspecified shoulder. Although there is no cure for this condition, several treat...

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