About Autosomal Recessive Spastic Paraplegia Type 35

Hereditary Spastic Paraplegia 35, also known as autosomal recessive spastic paraplegia type 35, is related to spastic paraplegia 7, autosomal recessive and mast syndrome, and has symptoms including ataxia, seizures and urgency of micturition. An important gene associated with Hereditary Spastic Paraplegia 35 is FA2H (Fatty Acid 2-Hydroxylase), and among its related pathways/superpathways are Autophagy and superpathway of coenzyme A biosynthesis III (mammals). The drug Iron has been mentioned in the context of this disorder. Affiliated tissues include globus pallidus, brain and subthalamic nucleus, and related phenotypes are spastic paraplegia and babinski sign

Major Symptoms of Autosomal Recessive Spastic Paraplegia Type 35

Autosomal recessive spastic paraplegia type 35, also known as Charcot-Marie-Tooth disease, is a genetic disorder that primarily affects children. It is characterized by progressive muscle stiffness and spasticity, as well as difficulty with mobility and balance. In addition, individuals with this condition may experience vision or hearing impairments, and some may have learning disabilities. The exact cause of Charcot-Marie-Tooth disease is not known, but it is thought to be related to a deficiency in dystrophin, a protein that helps keep muscles healthy. Treatment typically focuses on managing symptoms and improving quality of life, rather than curing the condition.

Suitable Lifestyle for People with Autosomal Recessive Spastic Paraplegia Type 35

The suitable lifestyle for people with Autosomal recessive spastic paraplegia type 35 varies based on individual differences and the severity of the condition, but here are some lifestyle suggestions that may be suitable for them:

1. Medical care: Patients need to receive regular medical examinations and treatments, Including spinal massage, rehabilitation training, drug treatment, etc.

2. Exercise therapy: Appropriate exercise can improve muscle strength and coordination, help reduce disability and maintain physical health. It is recommended that patients engage in low-intensity aerobic exercise, such as walking, swimming, cycling, etc. , and avoid high-intensity exercise to avoid causing more physical discomfort.

3. A nutritious and balanced diet: Patients need to consume adequate nutrients to support the body's recovery and maintain health. Patients are advised to follow the advice of their doctor or nutritionist and increase their intake of protein, vitamins and minerals.

4. Social interaction: Patients need to stay connected with family, friends and community to provide emotional support and social interaction.

5. Psychological support: Patients may face psychological pressure and difficulties, and it is recommended to seek professional psychological support and guidance. Every patient's situation is different, and a lifestyle plan that suits them should be developed based on their individual circumstances and their doctor's recommendations.

Other Diseases

Autosomal Recessive Spastic Paraplegia Type 54 Spastic Paraplegia Type 7 Hereditary Spastic Paraplegia Autosomal Recessive Bestrophinopathy Autosomal Recessive Congenital Ichthyosis Autosomal Recessive Hypophosphatemic Rickets Autosomal Recessive Polycystic Kidney Autosomal Recessive 2 Primary Hypertrophic Osteoarthropathy Autosomal Recessive 1 Primary Hypertrophic Osteoarthropathy Autosomal Recessive Isolated Ectopia Lentis

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