Nonne–Milroy disease

Nonne–Milroy disease is a rare, genetic disorder characterized by lymphedema, primarily affecting the lower limbs. The condition is congenital, meaning it is present from birth, and is caused by mutations in the FLT4 gene. Nonne–Milroy disease is a form of primary lymphedema, which refers to lymphedema that occurs on its own, not as a result of another condition or injury. This article provides an overview of Nonne–Milroy disease, including its symptoms, causes, diagnosis, and treatment options.

Symptoms

The primary symptom of Nonne–Milroy disease is lymphedema of the lower limbs, which often presents at birth or early childhood. Lymphedema is characterized by swelling due to the accumulation of lymph fluid, resulting from a blockage or malfunction in the lymphatic system. In addition to swelling, individuals with Nonne–Milroy disease may experience a feeling of heaviness or tightness, restricted range of motion, recurrent infections in the affected limbs, and changes in skin texture.

Causes

Nonne–Milroy disease is caused by mutations in the FLT4 gene, which plays a crucial role in the development and function of the lymphatic system. The FLT4 gene provides instructions for making a protein that is involved in the formation of lymphatic vessels. Mutations in this gene disrupt the normal development of the lymphatic system, leading to the symptoms associated with Nonne–Milroy disease. The condition is inherited in an autosomal dominant pattern, meaning only one copy of the altered gene in each cell is sufficient to cause the disorder.

Diagnosis

Diagnosis of Nonne–Milroy disease is primarily based on the clinical presentation of symptoms and a family history of lymphedema. Genetic testing can confirm the diagnosis by identifying mutations in the FLT4 gene. Imaging tests, such as lymphoscintigraphy, may also be used to assess the structure and function of the lymphatic system and to rule out secondary causes of lymphedema.

Treatment

There is no cure for Nonne–Milroy disease, but treatment is available to manage symptoms and prevent complications. Treatment options include manual lymphatic drainage, compression garments, exercise, and skin care to prevent infections. In some cases, surgery may be considered to remove excess tissue or to improve lymphatic drainage. Early and consistent treatment can help manage the symptoms of lymphedema and improve quality of life for individuals with Nonne–Milroy disease.

See also

• Lymphedema
• Genetic disorder
• FLT4 gene

Nonne–Milroy disease Resources
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