Familial chondrocalcinosis, right hand digital illustration

Familial chondrocalcinosis, right hand Save


ICD-10 code: M11.141

Disease category: M11.14: Familial chondrocalcinosis, hand

Familial Chondrocalcinosis, Right Hand

Familial chondrocalcinosis, also known as calcium pyrophosphate deposition disease (CPPD), is a rare genetic disorder that affects the joints. Specifically, familial chondrocalcinosis in the right hand refers to the presence of calcium pyrophosphate crystals in the joints of the right hand.

Chondrocalcinosis occurs when there is an accumulation of calcium pyrophosphate crystals in the cartilage of the joints. While it can affect various joints in the body, this article focuses on its occurrence in the right hand.

Symptoms:

  1. Pain and swelling: Individuals with familial chondrocalcinosis in the right hand may experience pain, tenderness, and swelling in the affected joints.
  2. Reduced range of motion: The presence of calcium pyrophosphate crystals can lead to stiffness and limited movement in the right hand joints.
  3. Joint inflammation: Inflammation of the joints is a common symptom, causing discomfort and warmth in the affected area.
  4. Joint deformity: In severe cases, familial chondrocalcinosis in the right hand can lead to joint deformities, affecting the appearance and function of the hand.

Causes:

Familial chondrocalcinosis is primarily caused by genetic mutations that affect the body's ability to process calcium pyrophosphate. These mutations result in the deposition of these crystals in the joints, leading to inflammation and pain.

Diagnosis:

To diagnose familial chondrocalcinosis in the right hand, a thorough physical examination and medical history review are necessary. Additionally, imaging tests such as X-rays or ultrasound may be used to detect the presence of calcium pyrophosphate crystals in the affected joints.

Management:

While there is no cure for familial chondrocalcinosis, treatment primarily focuses on managing the symptoms and preventing further complications. Treatment options may include pain management strategies, physical therapy, and lifestyle modifications to reduce stress on the affected joints.

In conclusion, familial chondrocalcinosis in the right hand is a rare genetic disorder characterized by the accumulation of calcium pyrophosphate crystals in the joints. It causes pain, swelling, reduced range of motion, joint inflammation, and potentially joint deformity. Early diagnosis and appropriate management can help individuals with this condition lead a better quality of life.

Treatment of Familial chondrocalcinosis, right hand:

Treatment Options for Familial Chondrocalcinosis, Right Hand

Familial chondrocalcinosis, a rare genetic disorder, affects the joints, particularly the right hand. It is characterized by the deposition of calcium pyrophosphate dihydrate crystals within the joint cartilage, leading to inflammation, pain, and stiffness. While there is no cure for familial chondrocalcinosis, several tr...

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