Clinical, genetic and radiographic analysis of 108 patients with von Hippel-Lindau disease (VHL) manifested by pancreatic neuroendocrine neoplasms (PNETs). Surgery. 2007;142(6):814-8; discussion 8.e1-2. 17. Varshney N. A Review of Von Hippel-Lindau Syndrome.
(2009) Chronic traumatic encephalopathy in athletes: progressive tauopathy after repetitive head injury. J Neuropathol Exp Neurol 68: 709–735. doi: 10.1097/NEN.0b013e3181a9d503 PMID: 19535999 Smith DH, Johnson VE, Stewart W (2013) Chronic neuropathologies of single and repetitive TBI: substrates of dementia? Nat Rev Neurol 9:211–221. doi: 10.1038/nrneurol.2013.29 PMID: 23458973 Gardner A, Iverson GL, McCrory P (2013) Chronic traumatic encephalopathy in sport: a systematic review.
Sometimes it isn’t recognized for several years, it can go as far adulthood until a health defect can be noticed. 2. Premature births can alter with the baby’s intellectual and developmental progression causing problem with the functioning of the baby’s brain. i. This can delay the baby’s physical and learning development, its ability to communicate with others, and with the ability to care for itself.
Cleopatra went and refuged in a place she had built for herself. Around this time Mark Antony received word from a messenger that Cleopatra was dead. Because of this he stabbed himself with his own sword trying to commit suicide. Yet before he died another messenger told him that Cleopatra still lived. With this news Mark had himself carried and delivered to Cleopatra’s location.
Treacher Collins is a disease that is caused from a genetic mutation in the TCOFI, POLRIC, and POLRID gene. Some symptoms are slanted eyes, vision loss, and hearing loss. The Treacher Collins disease is not treatable but can be made easier for everyday life. Tests like the cleft palate repair, external ear surgery, and the zygomatic reconstruction sometimes make the lives of those with the syndrome better. Nothing else contributes to this disease because there is only one type of it that is non-treatable and it does not effect a person’s mental or brain health and growth.
Noonan Syndrome Having a family member or child with an uncommon condition can be pretty extreme. When it comes to these conditions, they are usually some sort of mutation or run in the family 's genetics. Noonan Syndrome is a rare condition that affects an individual 's physical appearance, mental state, and genetic makeup, but varies in each affected person. In 1963, Noonan Syndrome was first described by a heart-specialist, Jacqueline Noonan. Of course, the condition will most likely involve a heart problem, which is discovered at birth, along with a webbed neck, chest deformities, many birth marks, also known as café-au-lait spots, and a short stature.
The MTL/D patients will have difficulty in remembering new items while FL patients have no problem in it. Also, the source memory was not often correlated with neuropsychological measures of MTL/D function, but it was predicted by the measures of FL function. Two reports suggest that impairing of source memory by FL is not in the case of emotional situations. Patients with FL damage asked how they learned of the death of Princess Diana. (Kapur et al, 2000).
Genetics of childhood and adolescent depression: insights into etiological heterogeneity and challenges for future genomic research. Genome Medicine, 2(9), 68. http://doi.org/10.1186/gm189 World Health Ministers,(2001) Mental Health. Geneve: World Health
Lesch-Nyhan Syndrome A report by Okafor Gift Onyinye A student from the department of Molecular Biology and Genetics. Introduction The Lesch-Nyhan syndrome (LNS), was found by Michael Lesch and William Nyhan and has provided the first detailed clinical description of Lesch-Nyhan disease in 1964, is a rare inherited disorder transmitted as a sex-linked trait and caused by a deficiency of an enzyme of purine metabolism: hypoxanthine-guanine phosphoribosyltransferase (HGPRT). (1) Epidemiology The lesch-Nyhan disease, it is a rare genetic disorder that can be transmitted at birth. Estimate show that at birth it affect 1/380000 and 1/235000 live births. The lesch Nyhan syndrome is an x-linked recessive disease.
Retrieved from http://emedicine.medscape.com/article/1132465-overview Solomon, C., & Cohen, J. (2013). Herpes zoster. The New England Journal of Medicine, 369(3), 255-263. Retrieved from https://search-proquest-com.southuniversity.libproxy.edmc.edu/docview/1401480411?accountid=87314 Webmd.
Jennifer Koser Joe Sonsella General Psychology 4-22-16 Antisocial Personality Disorder (ASPD) is one of 10 personality disorders in the manual of mental disorders. It is commonly characterized by a person who consistently shows no regard for right and wrong, and ignores the rights and feelings of others. They tend to manipulate or treat others harshly, and show no remorse for their behavior.1 The criteria for diagnosing this disorder differs depending on the version and source, but usually requires a lifelong pattern of symptoms. Scientific evidence shows individuals displaying anti social behavior from a young age and remaining this way for the span of their life. The population of people with ASPD is diverse.
History: The Pt had Left Total Knee Replacement (TKR) ON 06/03/2015, following immense pain due to degenerative joint disorder. Pt had been having the pain since little over 5 years, but since the past year it started being unbearable as per the patient. Past Medical History: Pt has a Past Medical History (PMH) of Degenerative Joint Disease (DJD), back pain, anxiety, depression, GERD and hypothyroidism.
Introduction: Diabetes Insipidus (DI) is a common complication following pituitary surgery. It has been traditionally reported in the range of 5 to 15% after transsphenoidal resection of pituitary adenomas. Here we report our experience with Diabetes Insipidus following Endoscopic resection of pituitary adenomas. Methods: We retrospectively reviewed the Stanford University Pituitary Adenoma database. Between the years 2007 and 2012 we identified 183 patients who underwent endoscopic resection of pituitary adenomas by the senior author (G.R.H).