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Carpal Tunnel Syndrome - MedlinePlus Genetics

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Last Updated: 10 January 2023

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Carpal tunnel syndrome

Carpal tunnel syndrome is a disorder caused by neural function disruptions, resulting in pain and numbness, primarily in the wrist and hand. Although carpal tunnel syndrome can occur at any age, it most often affects people between the ages of 40 and 60. It is most often the hand used for writing when only one hand is affected, as it is not uncommon. The pain or paresthesia is usually felt in the wrist, the palm, and the first four fingers of the hand in carpal tunnel syndrome. Certain activities that stretch or stretch the wrist, such as driving, typing, or holding a telephone may be triggering carpal tunnel syndrome. People with carpal tunnel syndrome can have muscle and nerve wasting in the affected hand, as well as a reduced ability to detect sensations, which can be mistaken for a change in symptoms.

Source link: https://medlineplus.gov/genetics/condition/carpal-tunnel-syndrome


Hereditary neuropathy with liability to pressure palsies

Hereditary neuropathy due to pressure palsies is a condition that affects peripheral nerves. These nerves connect the brain and spinal cord to muscles, and sensory cells that detect touch, pain, and temperature. Typical episodes of numbness, tingling, and muscle loss in the region associated with the affected nerve, typically an arm, hand, leg, or foot, are typical. Pressure on a single nerve can cause a pressure palsy episode, and any peripheral nerve can be affected. Carpal tunnel syndrome is common among people with this condition, and it occurs when a nerve in the wrist is involved. The Carpal tunnel syndrome is characterized by numbness, tingling, and hand and finger weakness. These signs of hereditary neuropathy with connection to pressure palsies usually start in childhood or early adulthood, but can develop anytime from childhood to late adulthood.

Source link: https://medlineplus.gov/genetics/condition/hereditary-neuropathy-with-liability-to-pressure-palsies


Acromicric dysplasia

Acromicric dysplasia is a condition characterized by short stature, short limbs, stiff joints, and distinct facial features. Newborns with acromic dysplasia are of normal size, but premature growth has resulted in short stature. Adults with this disorder average height is about 4 feet, 2 inches for women and 4 feet, 5 inches for men, according to the average. Often people with carpal tunnel syndrome suffer from numbness, tingling, and weakness in the hands and fingers. In this condition, a misalignment of the hip joints can also occur. These skeletal and joint disorders may necessitate medical intervention, but most affected individuals have no restrictions in their daily activities. A round face, sharply defined eyebrows, long eyelashes, a bulbous nose with upturned nostrils, a long space between the nose and upper lip, and a narrow mouth with thick lips can be seen with a narrow lips.

Source link: https://medlineplus.gov/genetics/condition/acromicric-dysplasia


Mucopolysaccharidosis type II

Mucopolysaccharidosis type II, also known as Hunter syndrome, is a disorder that affects several organs of the body and occurs almost exclusively in males. People with MPS II tend to have thick skin that is not elastic. Some of the affected individuals have also noticeable white skin growths that look like pebbles. Most people with this disorder experience hearing loss and recurrent ear infections. Some people with MPS II have trouble with the light-sensitive tissue in the back of the eye and reduced vision. The spinal cord can be compressed and injured if the spinal cord is narrowed. Many people experience heart valve problems, and MPS II also affects the heart. Heart valve abnormalities can cause the heart to become enlarged and can lead to heart failure. Children with MPS II continue to grow steadily until about age 5, and then their growth stalls and they attain short stature. Multiple skeletal abnormalities seen on x-ray are present among MPs II's two most common conditions. While both types of cancer affect many organs and tissues, people with severe MPS II experience a decrease in cognitive function as well as a more rapid disease progression. Individuals with mild MPS II have a shorter life expectancy, but they do not live to adulthood, and their intelligence is not affected. People with both forms of MPS II die from heart disease and airway obstruction.

Source link: https://medlineplus.gov/genetics/condition/mucopolysaccharidosis-type-ii


Transthyretin amyloidosis

Transthyretin amyloidosis is a slowly progressive disease characterized by abnormal deposits of amyloid-soluble amyloid in the body's organs and tissues. Transthyretin amyloidosis is divided into three main types of transthyretin amyloidosis, which are characterized by their signs and body organs that affect it. Transthyretin amyloidosis, a peripheral and autonomic nervous system, is the most affected by the neuropathic route, resulting in peripheral neuropathy and trouble controlling bodily functions. Some people have heart and kidney problems as well. Multiple eye problems may arise, such as cloudiness of the clear gel that fills the eyeball, dry eyes, increased pressure in the eyes, or pupils with an irregular or'scalloped' appearance. Some people with this disorder develop carpal tunnel syndrome, which is characterized by numbness, tingling, and a lack of hand and fingers. Transthyretin amyloidosis, which is mainly related to the central nervous system, is the leptomeningeal form of transthyretin amyloidosis. Amyloidosis is most common in people with amyloidosis in the leptomeninges, which are two thin layers of tissue that cover the brain and spinal cord. Eye problems in the neuropathic form may also occur. When people with leptomeningetal transthyretin amyloidosis have eye problems, they are thought to have the oculomeningeal form. Transthyretin amyloidosis, a cardiac disease, affects the heart. An abnormal heartbeat, enlarged heart, or orthostatic hypertension may be present in people with cardiac amyloidosis. Occasionally, people with transthyretin amyloidosis have mild peripheral neuropathy.

Source link: https://medlineplus.gov/genetics/condition/transthyretin-amyloidosis


Mucopolysaccharidosis type VII

The most common cases of MPS VII are caused by hydrops fetalis, a condition in which excess fluid builds up in the body before birth. About half of babies with hydrops fetalis are either born or die soon after birth. Members of MPS VII also begin to exhibit signs and symptoms of the disease in early childhood. People with MPS VII may also suffer with recurring ear infections and hearing loss. Many children with MPS VII suffer from Carpal tunnel syndrome, which is characterized by numbness, tingling, and a lack of hand and fingers. People with MPS VII may experience a narrowing of the spinal canal in the neck, which can depress and damage the spinal cord. The severity of conditions determines the life expectancy of individuals with MPS VII. People with MPs VII are likely to die from heart disease and airway blockagation.

Source link: https://medlineplus.gov/genetics/condition/mucopolysaccharidosis-type-vii


Mucopolysaccharidosis type I

Children with MPs I rarely have no signs or symptoms of the disease at birth, though some have a soft out-pouching around the belly button or lower abdomen. People with severe MPS I generally start showing other signs and symptoms of the disorder within the first year of life, while those with the attenuated form have milder features that appear later in childhood. In some people with MPS I, the airway may become narrow, resulting in frequent upper respiratory infections and short pauses in breathing during sleep. People with MPS I often experience cloudy of the eye's clear covering, which can lead to significant vision loss. Some affected individuals may also suffer from hearing loss and recurrent ear infections. MPS I have short stature and joint deformities that affect mobility. Multiple skeletal abnormalities that were seen on x-ray will also be present in most people with the severe form of the disease. The spinal cord can be compressed and injured by narrowing the spinal canal in the neck. Although both types of MPS I can influence various organs and tissues, people with significant MPS I have a decrease in cognitive function and a more rapid disease progression. Attenuated MPS I usually live to adulthood and may or not have a shorter lifespan. In people with both types of MPs I, heart disease and airway obstruction are two leading causes of death.

Source link: https://medlineplus.gov/genetics/condition/mucopolysaccharidosis-type-i

* Please keep in mind that all text is summarized by machine, we do not bear any responsibility, and you should always check original source before taking any actions

* Please keep in mind that all text is summarized by machine, we do not bear any responsibility, and you should always check original source before taking any actions