What is Marfan Syndrome Marfan syndrome is a genetic disorder that affects the connective tissue in the body. Connective tissues are one of the most important parts of the body. Connective tissues holds together all of the body’s cells‚ organs and other tissues. The connective tissues play a major part in ensuring the proper growth and development throughout the body. Marfan syndrome affects a protein called fibrillin-1. Marfan syndrome is caused by a defect in the gene that tells the body how to
Premium Genetic disorder
Unit 67 1.1 Explain how the range of early years settings reflects the scope and purpose of the sector. There are many different types of childcare provision: *Mother and toddler group-this is a place where toddlers can socialise with other children of their own age whilst the mother and father can stay‚play and learn more ways to look after and help with their childs development *Pre school-Is a private nursery‚one that is paid for by the parents and children from 3 years can get 15 hours free
Premium Childhood Primary education School
Munchausen Syndrome by Proxy Munchausen Syndrome by Proxy is a serious disorder that is often looked over by many. It is a very serious disease and must not be taken lightly. Munchausen syndrome by proxy‚ also known as factitious disorder by proxy‚ is a form of child abuse where the mother or parent makes up or produces illnesses in their own child. Many cases of this disease have lead to the death of the child and imprisonment of the parent. This is a disease that needs to be made aware of and
Premium Medicine Physical abuse Child abuse
Alien Hand Syndrome This is a proposed neurological disorder that is characterized by the affected person’s own hand or hands that seemingly have taken over its own free will or mind of its own.. It happens when someone your hand moves alone. they are not in control of it as if it isn’t part of the body. It is believed that it is a result from a brain surgical intervention‚ in treatment of worst cases of epilepsy. Some reports would also say that this condition can be acquired after a cerebrovascular
Premium Causality Neurology Mind
The Long Range Imagine a place where the grass is short and wavy. Where the wind blows but‚ only slightly. Where the sun glistens off the ATV’s windshield as you cruise down the hill to set up the flag and the rigid ceramic target. Now‚ you drive back up to the top of the hill‚ adrenaline and excitement coercing through your veins. You grab the rifle out of the hard protective case. You admire the rifle’ smooth‚ precision edges its long‚ smooth barrel made of perfict steel.You take a deep breath
Premium
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
Premium Blood type Gene DNA
Review a range of assessments methods by Clare Arnold Without some kind of assessment then you will find it difficult to measure whether learning has taken place or not. The reasons for assessing is to find out if someone is capable of doing a course at a particular level or to see if they are ready to go on to the next level due to the higher level of work required. “Assessment is the process of obtaining information about how much the student knows and evaluation involves using that information
Premium Assessment Evaluation
Super Duper® Handy Handouts!™ Number 116 What is Down Syndrome? by Becky L. Spivey‚ M.Ed. What is Down syndrome? Down syndrome is a congenital disorder stemming from a chromosomal abnormality appearing in one of every 800 births. It is the most common genetic disorder affecting more than 5‚000 babies born in the United States each year. This syndrome occurs when one chromosome has an extra “part‚” an error occurs in cell division‚ or an extra chromosome exists resulting in 47 chromosomes. Most
Premium Down syndrome Chromosome
Lesch Nyhan Syndrome Lesch Nyhan Syndrome (LNS) was first reported in 1964 by Michael Lesch and William L. Nyhan. It is a rare disorder located on the x chromosome. It is a sex-linked trait‚ which means that it is passed from mother to son. This condition can be inherited or occur spontaneously as a result of a genetic mutation. It usually appears once in every 100‚000 male births. Since the defective gene is recessive‚ females almost never exhibit symptoms of the disease. However‚ they can be
Premium Kidney stone Uric acid
Polycystic ovary syndrome (PCOS) or Stein-Leventhal syndrome‚ is an endocrine disorder in women that has varying degrees of early and long-term reproductive and metabolic risk. PCOS is the most common female endocrinopathy during childbearing age with around 6%-10% of the population afflicted. (Palomba et al.‚ 2015). While many that have been diagnosed with PCOS have ovarian cyst‚ it is not the symptom required for diagnoses. To be diagnosed with PCOS one must be afflicted with at least two of three
Premium Menstrual cycle Pregnancy Obstetrics