This case provided an excellent example of how the initial working diagnosis can change over time as further clinical, radiological and haematological information is obtained from specialised investigations. It also illustrates that association is not always causation i.e. the head injury coincides with symptom onset, yet there was no evidence of cerebellar injury on imaging. The complex nature of each individual’s health can be seen in this young patient. Rarely does a health problem present according to the “textbook” definition, nor do problems exist in isolation. Many patients present with one issue but have an underlying condition, such as anaemia, unearthed during investigations. Acute Ataxia This patient’s likely diagnosis is acute ataxia, a relatively uncommon condition with an incidence of 1 in 100,000. Acute ataxia is the sudden loss of voluntary, coordinated muscle …show more content…
Acute cerebellar ataxia in children is a self-limiting disorder which typically resolves within 5 to 12 days. The outcome of the condition is determined predominantly by aetiology. 90% of children recover without any neurologic sequelae with 10% having some long-term neurological problems. Current recommendations state that a child does not require hospitalisation provided all serious causes of acute cerebellar ataxia have been ruled out. Conservative management is the preferred treatment. All children need clinical re-evaluation 2 weeks following the initial presentation of symptoms. If the child’s symptoms persist, worsen, or if new symptoms appear during this time, investigations for other causes of ataxia are necessary. Diet and Anaemia in Children During the investigations of the patient’s ataxia, it was discovered that Master A.B. had a hypochromic, microcytic anaemic. • Haemoglobin → 6.8 g/dL, • Mean Corpuscular Volume → 76.8 fL, • Mean Corpuscular Haemoglobin → 22.5
However, after that, her friend noticed that Sam didn’t look well and acted unusually. At the primary observation, she complained a continuous headache, nausea, dizziness and blurred vision. She has a history of a concussion 1 year ago. Physical examination / Vital signs + pain assessment Physical examination includes inspection for signs and symptoms associated with the injury and significant history in relation to intracerebral
He was never told blows to the head could cause long term damage nor has he asked for compensation for injuries sustained. One of last questions asked at the end of frontline’s interview asks the pathologist who has studied the brains of deceased football players and the findings. “Would you allow your child to play football knowing what you know now”? Her answer,
Infants can lose motor skills such as crawling, sitting, or turning over. There is a milder form of Tay-Sachs called late-onset Tay-Sachs which causes muscle weakness and
According to her book, with an increase in sports affiliated concussions among children, it has become necessary for practitioners to understand how to go about handling age appropriate assessment, diagnosis, and treatment of the concussions. It is also critical
As the condition is only diagnosable post-mortem, it is unknown how the repeated head injuries that much of our youth experience are effecting their development. In being unable to diagnose CTE in the living, there is no way to know how these repeated traumas are affecting the development of a growing brain. We have only been able to see the effects of CTE on those who have passed, and there is no way to determine at what point the condition began to take hold. This bigger, faster, and stronger generation may be set up for failure as the prevalence of concussions is on the rise, with no way to detect or prevent future
ALS and CTE is a very serious topic, and many haven’t joined the conversation or don’t know much about the two subjects. In the sports world, many athletes are being diagnosed at a very young age with these awful diseases. I believe that in order for the number of athletes being diagnosed to drop, they must further their knowledge on the subject. ALS which stands for Amyotrophic Lateral Sclerosis, is a neurodegenerative disease that attacks the nervous system. ALS is also known as Lou Gehrig’s Disease because of the famous New York Yankees baseball player Lou Gehrig, Gehrig had a strong bad and was on of the best first baseman’s.
People cannot diagnose CTE until an autopsy has taken place, and they diagnose it with Tau protein. CTE is believed to have four stages that affect the human body. These stages are dangerous because many victims think it’s normal aging, and then they catch it too late (“What is CTE”). The first stage might not come until months to years after the head trauma. This stage includes bad headaches and
Breaking down the disease “amyotrophic lateral sclerosis” word for word can help you understand how this disease affects someone. The word “Amyotrophic” comes from the Greek language. “A” means no, “myo” refers to the muscles, and “Trophic” means nourishment. This translates to “No muscle nourishment.” When a muscle has no nourishment it wastes away and cannot be used.
In order to be diagnosed with a concussion or brain injury, you need to have a neurological exam. This will likely occur in the emergency room by a physician. If they believe that you may have had a concussion or a more serious injury, they will likely order a series of more definitive testing, such as CT or MRI scans of the brain. A neurologist or radiologist will read the scans and determine the extent of the damage. Once it 's determined the person has in fact experienced a concussion, a variety of treatment options will be suggested.
In recent years, doctors have worked to determine how dangerous concussion actually
If the student’s symptoms last longer than 7-14 days, a medical provider should consider referring the student for an evaluation by a neuropsychologist, neurologist, physiatrist, or other medical specialist in traumatic brain
For children, spending less time in recovery after coma is essential, it’s not sufficient enough to recover from a coma, but it is crucial that patients suffer no neurological issues (Karma & Rawat, 2006). Occupational therapy is important for an early and speedy recovery in order for the patient to be treated with the appropriate methods of healing. A physical disability such as TBI, “encompasses a wide range of severity from mild to severe” (Powell, 2016, p.1). Since TBI sustains a wide spectrum of injuries, occupational therapy has different methods that can be useful in completing the patient’s treatment. According to Janet Powell, the main injuries for TBI are falling, car accidents, or blunt force trauma to the head (Centers for Disease Control and Prevention, 2015, as cited by Powell, 2016).
Treatment programs need to include special education and vocational training components that emphasize skills leading to the patient functioning in society in the least restrictive, but safest possible environment. Prevention of FAS is the most effective treatment. The cost is astonishing for the long term care of children who have FAS or FAE. In Alaska Senator John Binkly estimated the cost at over 1.4 million dollars over the life span of the individual. Multiple this estimated cost by about 40,000 children a year born with FAS or FAE and the cost is huge.
According to WebMD, the first type of spinal muscular disease is the most serious variant due to the fact that most children with type 1 fail to live past two years of age from breathing issues because the muscles that control breathing are feeble. Symptoms of type 1 include limp arms and legs as well as the trouble swallowing. Moreover, type 2 spinal muscular atrophy occurs with children from six to eighteen months old. According to the National Organization for Rare Diseases, children with type 2 are able to sit on their own, but fail to walk more than 10 feet, however, once they mature to a teenager, they will be unable to sit independently. A symptom common for people diagnosed with type 2 is the fingers quivering (National Organization for Rare Diseases).
The infant may develop temporary muscle weakness and associated findings (i.e., transient neonatal myasthenia gravis). The passage of anti-acetylcholine receptor antibodies through the placenta to the unborn child during pregnancy may cause this condition to the infant. Some of the myasthenia gravis is inherited as an autosomal recessive, or more rarely, an autosomal dominant condition is described as congenital myasthenia gravis. The individual that inherits two copies of an abnormal gen for the same trait from each parent, the individual will have recessive genetic disorders. If the individual receives one normal gene and one gene for the disease, the person will be a carrier for the disease but usually will not show symptoms.