Klippel–Feil syndrome is a very rare disease. It was reported for the first time in 1912 by Maurice Klippel and André Feil. It has been characterized by the fusion of any 2 of the 7 cervical vertebrae. The syndrome occurs in a heterogeneous group of patients unified only by the presence of a defect in the formation or segmentation of the spine. Klippel–Feil syndrome can be identified by shortness of the neck. Those with the syndrome have a very low hairline and the ability of the neck to move is
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Appellate Courts v. Lower Courts State Court Systems have a unique two tier structure‚ which is broken down into specialized courts. Each branch of these structures have their own unique set up and hear different types of cases. Some have different guidelines‚ boundaries‚ and laws they must abide by‚ but ultimately the highest court in a state is the Supreme Court and the lower being a mayor or magistrate court. Federal Court have their own system with a similar tier structure to it‚ but is made
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Neonatal abstinence syndrome is a combination of neurologic‚ gastrointestinal‚ and autonomic dysregulation symptoms. This combination makes it difficult to deal with in an absence of medication. Methadone‚ a synthetic analgesic opioid. Similar to morphine effect‚ but less in sedation severity‚ considered as the gold standard treatment in pregnancy opioid abstinence‚ since around 45 years. As metabolism accelerate in pregnancy‚ Methadone’s effect end faster than in non-pregnant women. This make both mother
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Marfan syndrome is a multisystem disorder resulting with clinical manifestations typically involving the skeletal‚ ocular‚ and cardiovascular systems. Skeletal abnormalities of Marfan syndrome include disproportionate overgrowth of the long bones‚ anterior chest deformity due to overgrowth of the ribs‚ and overgrowth of the fingers. A reduced upper-segment to lower-segment ratio to arm span to height ratio of greater than 1.05 due to the overgrowth of the arms and leg is also a major criterion for
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April 30‚ 2005 Micro. Comp. Shaken Baby Syndrome Imagine yourself as a sweet‚ innocent‚ precious little baby. You are totally dependent upon adults to give you what you need and most importantly love. Your only means of communication is crying so you cry when you need to be fed‚ when you need your diaper changed‚ when you aren’t feeling so well‚ or when you just want some attention. You are crying and someone comes over to you. They pick you up‚ but instead of holding you and comforting
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general adaptation theory (GAS). [pic] The General Adaptation Syndrome (GAS) In order to develop a general theory for the physiological response of humans and animals to stress‚ Hans Selye‚ former director of Experimental Medicine and Surgery at the University of Montreal‚ performed an integrated analysis of the effects of stress on adrenal gland function. He called his model of stress adaptation the General Adaptation Syndrome or GAS. The GAS was thought by Selye to outline how the organism
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advantages and disadvantages? Budd Chiari Syndrome •Clinical term used to describe the manifestation of hepatic venous outflow obstruction •Secondary to hepatic vein thrombosis •Or to the narrowing/occlusion of the inferior vena cava (Khan 2009‚Val DC 2003) Ostial stenosis web thrombus Abdominal vein Liver Stomach Gallbladder Enlarged caudate lobe Inferior vena cava Portal vein (Menon et al.‚ 2004) Budd Chiari Syndrome • Primary type -Endoluminal venous (I.e. Thrombosis
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1. Explain what must happen in order for Greg and Susan to have a child with O type blood and nail-patella syndrome. Greg needs to pass down his chromosome 9 which carry the alleles‚ n and i. Susan also has the n and I alleles on chromosome 9. If both these alleles from both parents are passed down‚ it will create the allele Nnii which produced the blood type O and nail patella syndrome. 2. Determine all possible parental and recombinant gametes produced by Greg and Susan. Greg’s parental
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How foreign is Foreign Accent Syndrome? Christina Stone ENG101 Mr. Link Tuesday October 30‚ 2012 Foreign Accent Syndrome is a rare medical disorder in which a patient develops what sounds like a foreign accent. Further investigation reveals a significant increase in the number of cases over the past few years. This essay will consider some of the reasons why Foreign Accent Syndrome also known as FAS has had such a rapid escalation. The question of whether FAS is
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Diarmuid Sugrue Angelman Syndrome SYMPTOMS Angelman Syndrome is a neuro-genetic disorder involving the chromosomal region 15q‚ between positions 11-13. The symptoms primarily include intellectual development retardation‚ epilepsy‚ speech impairment‚ ataxia‚ and persistent laughing or smiling. CAUSATIVE MUTATIONS A healthy individual receives 2 copies of the 15 chromosome‚ one maternal and one paternal. The chromosomal region 15q11-13 (base pairs 23‚133‚488-23‚235‚220)‚ contains the gene
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