10 early signs and symptoms of muscular dystrophy

10 early signs and symptoms of muscular dystrophy

Muscular dystrophy is a term used for a group of genetic disorders that affect an individual’s muscles, resulting in progressive muscle weakness and degeneration. The condition is usually caused when the body is unable to produce muscle-building proteins because of certain abnormal mutated genes. Muscular dystrophy can emerge at any age, and recognizing its early signs and symptoms is pivotal for timely intervention and management. Here are the telltale early signs of the condition that should prompt one to seek expert help immediately.

Delayed motor milestones
In infants and young children, a delay in achieving motor milestones can raise concerns about muscular dystrophy. These milestones include sitting up, crawling, and walking. Children with muscular dystrophy may take longer to reach these developmental stages or exhibit unusual movement patterns when they achieve them.

Muscle cramps and pain
Apart from abnormal shortening of muscles and range of motion, muscle cramps and pain can also be early signs of muscular dystrophy. Individuals with this condition may be unable to move their joints freely and often experience persistent muscle cramps, which can be uncomfortable or even painful. One may experience these symptoms during physical activity or at rest.

Muscle weakness
This is one of the primary signs that affects the way an individual performs routine tasks requiring muscle strength, including lifting objects, climbing stairs, or getting up from a seated position. Initially, this weakness may be subtle and easily overlooked, but it tends to worsen over time.

Progressive muscle loss
If one notices one’s muscular mass shrinking with time, it can be a sign of muscular dystrophy. This change is more obvious around limbs, shoulders, and hips.

Frequent falls
Muscular dystrophy can bring balance issues in individuals due to weakened leg muscles. As a result, one may have a swaggering walk, issues with running, walking, or lying down, and seem unable to walk on toes. In children, parents may notice their child frequently falling, unable to jump or walk normally, or having difficulty keeping up with peers during physical activities. One is advised to observe any unusual changes in one’s walking pattern without any reason, which can serve as a valuable clue for early diagnosis.

Learning difficulty
Muscular dystrophy can cause learning disorders and delayed growth in kids. It’s advised to seek immediate professional help if one detects any early signs in kids for prompt treatment.

Large calves and curved spine
Both kids and adults with muscular dystrophy may have fatty deposits around their calves instead of muscles, making their calves look unnaturally big or swollen. Weakened muscular strength can also cause a curved spine, medically termed as scoliosis.

Vision issues
At times, the condition can also affect one’s eyesight, leading to dropping eyelids and vision problems. One’s facial muscles may also feel weak.

Difficulty in breathing and swallowing
Some forms of muscular dystrophy can affect the muscles responsible for breathing and swallowing. Early signs may include shortness of breath during physical exertion or difficulty swallowing solid foods. These symptoms can become progressively more severe as the condition advances.

Heart problems
Muscular dystrophy can also lead to respiratory issues and even heart conditions like arrhythmia, marked by irregular heartbeats, and cardiomyopathy, which results in weakened heart muscle function and even heart failure.

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Understanding arthritis – A common joint condition

The joints are constantly working while we move our limbs, so, understandably, people may develop certain joint conditions that cause pain and compromise mobility, especially with age. One of the common joint conditions is arthritis, which leads to joint inflammation and mild to severe pain. While there are several types of arthritis, the two most common types are rheumatoid arthritis and osteoarthritis. Stages Rheumatoid arthritis has four stages: Stage 1: At this stage, inflammation occurs inside the joints, and swelling, stiffness, and joint pain are the common symptoms. Stage 2: The inflammation of the joint lining, synovium, aggravates at this stage and results in cartilage damage. The affected joints’ range of motion is also compromised, causing pain and discomfort. Stage 3: At this stage, the severity of the joint condition increases, and it leads to bone damage. This results in more pain, loss of mobility, and weakness of muscles. The bones rubbing against each other can cause bone deformity as well. Stage 4: This is the final stage where the joints stop functioning completely. It leads to more pain, stiffness, and swelling, and the bones may even fuse, which is known as ankylosis. Osteoarthritis also has four stages of progression: Stage 1: Wear and tear may affect the knee joints, and minor spur growths on the affected bone can also be seen, but the condition does not cause too much pain at this stage. Stage 2: The bone spur growths increase and cause pain, and the knee joints become stiffer. Stage 3: This stage is characterized by joint inflammation leading to increased pain and stiffness. Walking can also cause popping sounds in the joints. Stage 4: The space between the bones in the joints becomes very narrow, causing the cartilage to wear down. Also, a chronic inflammatory response caused by the breakdown of cartilage aggravates discomfort and pain. Diagnosis of arthritis These joint conditions can be diagnosed using several tests. A physical examination reveals whether a patient has red, warm, and tender joints, and this test also helps examine the fluid around the joints. A rheumatologist can analyze the level of inflammation in the joints to determine the type of arthritis an individual is affected with. Also, blood tests are undertaken to check for antibodies like anti-CCP, rheumatoid factor, and antinuclear antibody. In addition, X-ray, CT scans, and MRI are also performed to check the condition of the cartilage and bones. Prevention of arthritis A family history of joint conditions like arthritis or aging can increase one’s risk of developing arthritis, but making certain lifestyle changes can also help lower the chances of developing the condition. To start with, one should include more foods with omega-3 fatty acids in their diet as these healthy fats are anti-inflammatory. One should also exercise regularly, keep their weight under check, reduce stress on their joints, and try to avoid injuries. Also, if one notices any symptoms of arthritis, they should consult a doctor immediately as early diagnosis goes a long way in managing the condition effectively through timely treatment.

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8 early signs and symptoms of narcolepsy

Narcolepsy is a chronic yet rare neurological disorder characterized by significant disruptions in one’s sleep patterns. Here, one’s brain cannot control one’s sleep and wake cycle, which in turn affects multiple aspects of an individual’s life, including health and daily routine. Narcolepsy is usually life-long, so understanding its symptoms is important for timely diagnosis and for developing effective strategies to manage it. Here are some signs that should prompt one to seek medical help. Excessive sleepiness during daytime Individuals with narcolepsy often feel an overwhelming urge to sleep throughout the day, regardless of how much sleep they received the previous night. This persistent drowsiness can be disruptive to daily life, causing difficulties at work or in school and posing safety risks in activities like driving. Muscular weakness Also known as cataplexy, one may experience a sudden and temporary loss of muscle tone, leading to muscle weakness or even complete collapse. These episodes are usually triggered by strong emotions like laughter, excitement, or anger. Not all triggers lead to cataplexy, but when it does occur, it can be a strong indicator of the disorder. Sleep paralysis Narcolepsy may also manifest as sleep paralysis, which is a temporary inability to move or speak while falling asleep or waking up. These episodes can be accompanied by vivid hallucinations, making them particularly frightening. Sleep paralysis can occur in isolation or be part of a larger narcoleptic episode. Hallucination and Rapid Eye Movement (REM) Narcolepsy individuals often experience vivid dreams, even during brief naps. In some cases, REM sleep, which is typically associated with deep, restorative rest, can intrude into wakefulness, causing dream-like experiences or hallucinations. This phenomenon is known as REM sleep intrusion and contributes to the disrupted sleep patterns seen in narcolepsy. Fragmented nighttime sleep Many individuals with narcolepsy find it challenging to maintain a consolidated nighttime sleep schedule. Usually, a person with a regular sleep cycle goes through four stages of the sleep cycle, from light to deeper sleep, then slow wave and REM sleep, with about 90 minutes of transition between each cycle. For narcoleptics, however, the cycle is disruptive. They may wake up frequently throughout the night or have difficulty falling asleep, which compounds their daytime sleepiness. Forgetfulness Narcolepsy can lead to lapses in attention during any normal activity and cause forgetfulness or amnesia. One may find it difficult to recall the activity one was performing before falling asleep. In addition, individuals with narcolepsy may spontaneously utter incoherent or unrelated words, often with the subsequent inability to recall them. Decreased alertness Individuals with narcolepsy may have generally decreased alertness, which goes beyond the occasional tiredness, leading to reduced productivity at work or school. Microsleep episodes Microsleeps are brief, uncontrollable periods of sleep that can last for a few seconds to a few minutes. This can include head drooping, blank stares, sudden body jerks, and an inability to keep eyes open. Narcoleptics may experience these episodes during activities like talking, driving, or working, leading to lapses in attention and increased accident risks. The exact cause of narcolepsy is not fully known, but researchers believe it is primarily associated with a deficiency of a neurotransmitter called hypocretin (or orexin), which plays a crucial role in regulating wakefulness and sleep. Genetic factors, hormonal changes, or autoimmune reactions can cause this deficiency. With proper medical guidance and support, individuals with narcolepsy can manage their condition and regain control over their lives.

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