Congenital disorder

Everyone has their own story and different journey of lives and I always believed that every story has their own unique and personal reasons. I don’t know where to start my story because I’m a person who is always bottle things up and I can't talk to anyone. Without confidence and courage, I have waited for the right time to write, to tell my story and to confess how I feel like everyone else. I’m the oldest and have two youngest sisters. We have always had our parents who love and care about us

principles serve as the foundation of nursing practice, education, and research (Colley, 2003; Antipuesto, 2011). This paper’s purpose is to elaborate on the author’s discussion of her phenomenon of interest (POI) on newborn screening for Critical Congenital Heart Defects (CCHD). The objectives of this paper are to discuss the metaparadigm of nursing as it relates to the author’s POI, to discuss the Neuman system model and discuss the POI within its framework, to discuss the inter-related concepts in

signals to an area of the heart called the pacemaker. (Pearson 2011, p.100-111). Even though the heart is the most vitalist organ in the human body, which carries rich nutrients and oxygen, defects can occur. The most common defect that occurs is a congenital heart defect, which is commonly known as a hole in the

Children with congenital heart disease (CHD) are at increased risk for psychosocial issues, decreased quality of life and decreased resilience. The standard of care for children with CHD cared for in the Heart Transplant and Heart Failure clinic did not include routine screening for psychosocial issues with a standardized tool. The purpose of this Doctor of Nursing Practice (DNP) project was the implementation of a protocol that screened children followed in this clinic for psychosocial issues, quality

most cases, the hole repairs by itself so you would not notice that you even had such a defect. In severe cases , surgery has to follow, if not, it can be fatal. I will be explaining how ASD affects the circulatory system. Effects of Atrial Septal Disorder As there is a hole in the wall separating the atria, the oxygenated blood from the left atrium enters the right atrium instead of the aorta. The oxygenated blood that entered the right atrium mixes with the deoxygenated

without any health complications, so to hear that your child was born with a congenital disease has to be hard to handle. In many cases, a child can live an enjoyable life with a congenital disease, such as dwarfism. There are many types of dwarfism beginning with the most common types to the rarest with Achondroplasia, Spondyloepiphyseal Dysplasia, and Diastrophic Dysplasia. To begin with, Achondroplasia is a disorder of bone growth (Learning About Achondroplasia, n.d.) and is the most common type

Introduction Congenital Insensitivity to Anhidrosis (or CIPA) is a rare genetic disease with the characteristics of not being able to feel any pain or temperature, and little or no sweating. It is inherited by an autosomal recessive pattern, meaning that both parents have a mutated NTRK1 gene, but they do not show any symptoms of CIPA. The damaged NTRK1gene produces proteins that cannot transmit signals. Since the neurons do not get any signals from the proteins, they perform apoptosis. Apoptosis

Nathalie Dao Med 2047 Ankylosing Spondylitis Instructor Michelle Earixson-Lamothe 12/04/2014 Definition Ankylosing Spondylitis is a form of arthritis; it is a chronic and progressive form of joint formation that usually affects the spine and the sacroiliac joints. The sacroiliac joints are located in the lower back where the sacrum, the bone directly above the tailbone meets the iliac bones, bones on either side of the upper buttocks. Over time, chronic inflammation of the spine, also known as

Dysphasia Uncommon hereditary disorder resulting in spinal malformations, growth deficiency, and occasionally ocular abnormalities. Spondyloepiphyseal Dysphasia Though not common has two types, known as Spondyloepiphyseal Dysphasia Tarda, and Congenital Spondyloepiphyseal both are a usual cause of short stature. Spondyloepiphyseal Dysphasia Tarda Predominantly effects men or boys typically distinguished as dwarfism, curved or hunched spine, this form of genetic disorder doesn’t usually become evident

disabilities can be either congenital or acquired after birth due to an accident or disease. 2.2 Describe the following terminology used in relation to physical disability: Congenital Acquired Neurological A congenital disability is a medical condition which you are born with, congenital disorders are caused by development problems with the fetus before birth, congenital disorders are also genetic and can be passed down from one or both parents. Examples of congenital disabilities: • Cerebral