Growth Hormone Syndrome Analysis
Recommended: Growth hormone
Case Study 1 – The Endocrine System Christina D’Amico University of Saint Joseph Abstract A fifteen-year-old boy with many hormonal abnormalities starting at the age of eleven suffered from joint pain and swelling along with poor bone growth and development. He broke his left hip and had low levels of testosterone and high levels of growth hormone resulting in gigantism and later acromegaly.
After a few years, there was a tumor in her pituitary region. The tumor was secreting excessive amounts of growth hormone, casing symptoms to appear. She had enlarged hands and feet, coarsened, enlarged facial features, coarse, oily, thickened skin, and
Tina Jones Medical Genogram Nessrin Leonida School of Nursing Course Number: Nurs516 January term of 2017 Tina Jone’s Medical Genogram Tina Jones is a twenty- eight year old, African American, who was diagnosed with asthma when she was two. She verbalized that cats and dust trigger her asthma. She did have chicken pox as a child, and also has type two diabetes in her twenties. Tina’s paternal side consists of her grandfather, who died five years ago at the age of sixty- five due to colon cancer. He has a history of type two diabetes.
Other symptoms for DMD include pseudohypertrophy (the growth of an organ or a part due to an increase in the amount of other tissue that is fatty
When on the topic of murder trials, one cannot help but imagine the poor moral values of the attorney defending the suspected evil doer, but we hardly ever wonder rather or not the attorneys are mentally effected themselves. More often than not, most attorneys can find themselves alone with the dark secrets of their wicked clients. This is due to a client’s right in the justice system known as the attorney-client privilege. The attorney-client privilege is the client’s right to refuse to disclose and to prevent any other person from disclosing confidential communications between the client and the attorney. One well known example of just how far this “privilege” can go is the murder case of Robert Garrow.
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 features of this syndrome are not fully known, considering the fact that there are numerous characteristics and no two infected individuals have the same exact features. Like in most other disease cases, there are lists of more minor symptoms that can occur in an individual. In infants and newborns, feeding problems are present, due to a poor sucking reflex. Behavioral problems and developmental delays can occur, which causes the individual to achieve milestones slower, such as sitting and walking.
It often occurs in children who have one or both parents who were also slow to develop. SYMPTOMS Children with CGD tend to be a bit short in early childhood, but they grow at a normal rate. They do not have the rapid growth spurt of adolescence when other children their age do. They continue to grow but at a slow rate. They also do not show signs of puberty until later.
Lordosis is decreased. Lasegue’s is equivocal, bilaterally. There is positive straight leg raise at 70 degrees, bilaterally, eliciting pain in L5-S1 dermatome distribution. Physical exam reveals tightness and spasm of the paraspinal musculature, bilaterally. There is hypoesthesia at the anterolateral aspect of foot and ankle of an incomplete nature noted at L5, and S1 dermatome level, bilaterally.
There are multiple facial features that will occur when a child has FAS, however these symptoms will vary from child to child and depend on the severity of the condition. Children who suffer from FAS may have an extremely thin upper lip, smooth skin between the upper lip and the nose, a small, upturned nose, and small eyes. Other deformities can include slow physical growth after birth, vision and hearing struggles, deformities of the joints, limbs and fingers, have a small head and small brain size, heart defects, skeletal issues, and digestive
Thyroxine (T4) increases oxygen consumption in practically all tissues and thus increases the metabolic rate/ elimination of waste and consumption of oxygen. It is involved at many levels in growth and development. In fact hypothyroidism in infants can result in central nervous system and other systems to fail to develop normally. Excess throroxine in adults generally results in weight loss, nervousness, insomnia and elevated basal metabolic rate, with characteristic bulging eyes. In contrast hypothyroidism causes the individual to become sluggish in body movements, to put on weight, and a slowing down of mental
Most forms are from a random genetic mutation in either the father’s sperm or the mother’s egg rather than from either of the parent’s complete genetic makeup. Another cause of dwarfism is Turner Syndrome which is when a sex chromosome is missing or partially missing in girls or females and they inherit an X chromosome from each parent. Growth hormone deficiencies are also linked to genetic mutations that can result in dwarfism and some causes are just unknown. Dwarfism is typically defined as an adult height of 4 feet 10 inches or less and the average height among people with dwarfism is 4 feet. Dwarfism is usually divided into two categories; disproportionate dwarfism which is where some parts of the body are small and some parts are average or above average and this type prevents the bones from developing.
I observed a four year old girl that was tiny for her age. She worked on proprioceptive and vestibular input like the other children. One major difference is that her condition has not been diagnosed. The doctor suspect a chromosome issue, but her family has not gone for additional testing. Although she can recognize shapes, colors, and letters, she is still delayed.
Due to the fact that the character’s looks are never specified in Shakespeare’s a Midsummer Night’s Dream, it is up to the reader to decide what the characters look like. The main characters Demetrius, Lysander, Helena and Hermia all have distinct personalities that set themselves apart from each other. Demetrius is a noble with a fickle, and arrogant personality. His image has clothing lined with gold, a look of arrogance, and a fickle personality. First of all, Demetrius’ clothing is lined with gold and other jewels, around the ends of his clothing and boots.
Love can and can’t always conquer the unique stressors of an interracial relationship because an interracial relationship can consist of strong love that is unbreakable but under some circumstances, love can 't conquer all relationships due to cultural barriers and society. Depending on the relationship that people are in, others around them may support it while others may not. Some children feel pressured to live up to the expectations of their culture by dating someone within the same race. However, if they feel secure about their relationship they would not let anything destruct their love.
Molecular genetics have shown nearly all to be monoclonal, suggesting that an intrinsic pituitary defect is likely to be responsible for pituitary tumorigenesis. Occasionally, prolactinoma may be part of a multiple endocrine neoplasia syndrome (MEN-1), but this occurs too infrequently to justify MEN-1 screening in every patient with a prolactinoma. • GH- and PRL-secreting adenomas (or mammosomatotroph adenomas) Mixed growth hormone (GH)- and PRL-secreting tumors are well recognized and give rise to acromegaly in association with hyperprolactinemia.
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