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Osgood-Shlattard disease
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There are different types of knee diseases and Osgood-Schlatters Disease just happens to be one of them. OSD is an inflammation of the patellar ligament at the tibial tuberosity. It is characterized by a painful bump just below the knee and is occurs most often in young adolescents. The disease often occurs the most when a young child is involved with sports, such as soccer, basketball, figure skating, and ballet. While the disease is more common in boys, the gender gap is narrowing as more girls are becoming involved with sports.
What are the symptoms Each person with the disease varies. Some may only have mild pain performing certain activities, like running or jumping. For others, the pain can be unbearable. OSD can usually occur in one
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knee, but sometimes it develops in both knees. Discomfort can last from a couple of weeks to months and may recur until your child has stopped growing. Stress from sports can cause the tendon to pull away from the shinbone a bit, which results in the pain and swelling associated with Osgood-Schlatter disease.
In some cases, a child’s body may try to close the gap with new bone growth, which can result in a bony lump at the spot. During activities that involve a lot of running, jumping and bending – such as soccer, basketball, volleyball and ballet – when a child’s thigh muscles (quadriceps) pull on that tendon that connects the kneecap to the shinbone.
What are the risk factors The main risk factors for Osgood-Schlatters disease are – age: which occurs during puberty’s growth spurts; sex (gender): disease is more common in boys; and sports: condition happens most often with age in boys around the age of 13 to 14, and girls from the age of 11 to 12.
Are they complications from Osgood-Schlatters Disease? The complications are uncommon. Even after symptoms have resolved, a bony lump may remain on the shinbone in an area of the swelling. This lump may persist to some degree throughout your child’s life, but it doesn’t usually interfere with knee function. Knee pain will occur, swelling or tenderness, sometimes the pain will worsen with exercise or high-impact activities, or limping after physical
activity. How is Osgood-Schlatters Disease treated? Osgood-Schlatter disease usually resolves on its own once a growth spurt ends. Until then, treatment is focused on relieving symptoms, such as knee pain and swelling. Types of treatments includes – icing the affected area two to four times a day, or after doing physical activity; taking over-the-counter pain relievers, such as ibuprofen or acetaminophen; resting the knee or reducing physical activity; wrapping the knee or wearing a knee brace; stretching; or physical therapy. Some children may be able to participate in low-impact activities, such as swimming or biking, as they recover. Others may need to stop participating in certain sports for several months so their bodies can heal. Osgood-Schlatter disease usually doesn’t cause any long-term complications. Some children might also need surgery if the bone and tendons in their knee don’t heal correctly. Should you go see a doctor? More than likely, the attention will be brought to your family’s doctor. The doctor would highly recommend to go see a doctor who specializes in knee injuries or sports medicine. Tests and diagnoses are very important. There are x-rays that can be used to look at the bones of the knee and leg and more closely to examine the area where the kneecap tendon attaches of the shinbone.
1. James suffers from a condition called Duchenne muscular dystrophy. Explain the full meaning of this name.
Duchenne Muscular Dystrophy, also known as DMD, is the most common form of muscular dystrophy. Muscular dystrophy is a condition that is inherited, and it is when muscles slowly become more and more weak and wasted. Duchenne muscular dystrophy is a form of muscular dystrophy that is very rapid and is most commonly found in boys. In muscle, there is a protein named dystrophin. Dystrophin is encoded by the DMD gene. When boys have Duchenne muscular dystrophy, they do not produce enough dystrophin in their muscles. This causes weakness in their muscles. Parents can tell if their child has duchenne muscular dystrophy by looking for various symptoms.
Osgood-Schlatter Disease or syndrome (OSD) is an irritation of the patellar ligament at the tibial tuberosity (Dhar). Osgood-Schlatter Disease is claimed by some to not actually be a disease (Sims). But is rather a collection of symptoms that involve the tibial tubercle epiphysis (Sims). Osgood-Schlatter Disease affects as many as 1 in 5 adolescent athletes (Diseases and Conditions: Osgood-Schlatter Disease). Some other common names for this disease are Osteochondrosis, Tibial Aponphysitis, Tibial Tubercle Apophyseal Traction Injury, Morbus Osgood-
Osteogenesis Imperfecta (OI), also called fragile bone ailment or Lobstein disorder, is an inherent bone issue portrayed by weak bones that are inclined to break effortlessly with practically zero cause. A arrangement of various sorts of OI is regularly used to depict how seriously a man with OI is affected.OI is brought on by hereditary deformities that influence the body's capacity to make solid bones. In predominant established OI, a man has too little sort I collagen or a low quality of sort I collagen because of a transformation in one of the sort I collagen qualities which makes the bones
Emery-Dreifuss muscular dystrophy is a rare form of muscular dystrophy characterized by early onset contractures of the elbows, achilles tendons and post-cervical muscles with progressive muscle wasting and weakness It is also associated with heart complications like cardiomyopathy and arrhythmia which in both cases can lead to death. Cardiomyopathy is a heart disease which affects the muscles of the heart. In cardiomyopathy is muscles get rigid, enlarged or thick. They also sometimes changed by scar tissues. On the other hand arrhythmia is a disorder with the rhythm or rate of heartbeat. The heart can beat fast, which is called tachycardia or it could be beating too slow, which is called bradycardia. Emery-Dreifuss muscular dystrophy is characterized by early onset of contractures and humeroperoneal distribution. Humeroperoneal refers to effects on the humerus and fibula. The genes known to be responsible for EDMD encode proteins associated with the nuclear envelope: the emerin and the lamins A and C.
Clubfoot is a common congenital deformity of one or both feet. Clubfoot can sometimes be identified during fetal ultrasound or by visual inspection at birth. Physiotherapist Kelly Gray and Doctor Paul Gibbons describe clubfoot (Australian Family Practice (AFP), 2012) as “a deformity characterized by structural equinus (pointing down), adductus (turning in), varus (twisting, such that the heel is pointing in or upward), and cavus (high arch)” (p. 299). Skeletal abnormalities of clubfoot can include small calcaneus, navicular, and talus bones and a misshapen subtalar joint (Clubfoot, 2011). According to the Mayo Clinic (2013) the calf muscle of the affected leg is usually smaller than the non-affected leg, and the affected foot can be ½ inch shorter than the non-affected foot.
... and can lock the joints in painful positions. Often, teens are fitted with special braces to ensure flexible joints and tendons (the strong, rubber band-like tissues that attach muscles to bones). Surgery is sometimes used to reduce pain and increase movement from contractures.
An ankle fracture is a break in one or more of the three bones that make up the ankle joint. The ankle joint is made up by the lower (distal) sections of your lower leg bones (tibia and fibula) along with a bone in your foot (talus). Depending on how bad the break is and if more than one ankle joint bone is broken, a cast or splint is used to protect and keep your injured bone from moving while it heals. Sometimes, surgery is required to help the fracture heal properly.
Rixe JA, Glick JE, Brady J, Olympia RP. A review of the management of patellofemoral pain syndrome. The Physician And Sports Medicine. 2013;09:2023
It is estimated that 1 out of every 5,600-7,700 boys ages 5-24 have Duchene or Becker muscular dystrophy. (“Data & Statistics,” 2012 April 6) Muscular dystrophy is a group of genetic diseases defined by muscle fibers that are unusually susceptible to damage. There are several different types of muscular dystrophy some of which shorten the affected person’s lifespan. (“Muscular dystrophy: Types and Causes of each form,” n.d.) There is a long history of the disorder but until recently there wasn’t much knowledge of the cause. (“Muscular Dystrophy: Hope through Research,” 16 April 2014) Symptoms are obvious and can be seen as soon as a child starts walking. (“Muscular Dystrophy,” 2012 January 19) Although muscular dystrophy mostly affects boys, girls can get it too. (“Muscular Dystrophy,” 2012 January 19) There is no cure for muscular dystrophy but there are several types of therapy and most types of muscular dystrophy are still fatal. (“Muscular Dystrophy: Hope through Research,” 16 April 2014)
Congenital defects also may have genetic bases, as in families who have extra fingers or toes or in the disease osteogenesis imperfecta, in which children have such brittle bones that many are fractured. Disorders of growth and development include several kinds of dwarfism and gigantism. Bones or limbs may develop deformity as the result of known causes, such as the infection poliomyelitis, or unknown or variable causes, such as curvature of the spine (SCOLIOSIS) or CLUBFOOT. Infections Infections of bone, called osteomyelitis, are usually caused by pus-producing bacteria, especially Staphylococcus and Streptococcus.
Almost everyone develops osteoarthrits as they age, some get it while in their fifties and in others it does not appear until their eighties. Osteoarthritis is the most common form that affects older people; this form of the disease wears down the cartilage mostly through overuse and injury but there are other causes. This specific form of the disease causes the cartilage to break down and the bones to rub against each other. Deformity and swelling occurs because knobs of hardened bits of cartilage develop in the joint. It forms especially if a joint has been injured many times.
There are many muscles in the knee that a dancer uses for movement. One of the injuries that deals with the cartilage in the knee is Moviegoer's knee. Moviegoer’s knee is when the cartilage between the patella(kneecap) and the knee joint wears down . This condition can occur by poor body alignment or turnout. Another injury that deals with the knee is a Meniscus tear. A
There are many well-known disabilities and osteogenesis imperfecta is not one of them. Thus, this disability will be the topic of my investigation. Although osteogenesis imperfecta, also known as brittle bone disease, is not a widely-known condition, having knowledge on this rare condition will be helpful in case I encounter a child or adult with this condition. By having knowledge on rare conditions like osteogenesis imperfecta, better care and understanding can be provided to someone who is encountering this condition. All children and families deserve patience, understanding, and knowledgeable teachers, regardless if a child’s disability is well-known or not.