Gastroschisis Research Paper

Even though it's true that the health of your body and mind is largely determined by what you eat, your gut is in control of how the nutrients and energy in the food get into the rest of your body. Again, I'm giving a simplified model here, if you want to learn about gut health in more details, there are some books I recommend later on.

The development of IBD is very rare in infancy. Inflammatory bowel disease includes, Crohn disease (CD) and ulcerative colitis (UC). IBD manifests during childhood or adolescence in up to 25 percent of patients, however, a small percentage of children may present with IBD in infancy. A published data from epidemiological studies and IBD registries in North America and Europe showed that less than one percent of children with IBD present during the first twelve months of life. Even though the numbers are small, Crohn’s disease is more prevalent than ulcerative colitis in these and other studies. It is also common among infants initially diagnosed as ulcerative colitis or indeterminate colitis to have their diagnosis changed to CD during subsequent follow up. IBD with onset in this age group is likely a heterogeneous group of disorders, and has variability in the clinical presentation and prognosis (Kappelman & Grand,

The condition occurs when the anus does not develop normally in the womb. However, no one knows just why this happens. Often, babies born with this condition have other birth defects.

The paper attempts to find any correlation/connections between Hirschsprung Disease and Congenital heart disease. This was done by identifying children with Hirschsprung disease, which is a disease that causes the colon of the affected person to infllamme. Hirschsprung is Congenital,present at birth, and becomes an issues as the child mature, since passage of stool becomes difficult. This issue can be corrected but issues can arise when dealing with other diseases such as congenital heart disease. Some patients cases seem to imply that in attempting to solve the issues the patient is then affected long term. The study took place in a pediatric surgery center, in which 53 out of 61 children were chosen to take place of the study. All of these

One of the most important determinant of fetal viability is the pulmonary system development and maturity. The prenatal awareness of any abnormalities or anomalies going to ensure better management of the pregnancy, also giving the opportunity for the medical team and parents to prepare for the delivery and postnatal treatment. Congenital malformations of the fetal thorax are common which can involve many organs. Early detection and accurate diagnosis of fetal pathology are possible by using ultrasound and MRI imaging.

Hirschsprungs is a disease that is related to chronic constipation and usually manifests itself in early childhood, especially under the age of one. However, older children can have this disease as well, and some can even be born with this. Even though the younger children can have Hirschsprungs, it is not usually diagnosed until their later years due to the fact that children frequently have constipation and the need for enemas and laxatives when they are younger. Hirschsprungs is usually suspected when the child has had a more frequent need for enemas, and laxatives. A research study was done in order to examine the frequency of Hirschsprungs in the population as well as types of patients who were diagnosed with the disease.

Hirschsprung's disease is a birth defect. It results in the intestine becoming obstructed. Before 1948 infants with Hirschsprung's disease died (Hirschsprung's Disease"). Now with treatment, babies with the disease can survive. The disease is defined by its history, symptoms and diagnosis, and treatment. Hirschsprung's disease is a life-threatening birth defect that causes problems with bowel movements but with treatment available today the result is very good.

Hirschsprung disease is a congenital digestive condition primarily found in newborns, although older children can be diagnosed with mild cases. Damage to the nerve cells found in between the muscle layers of the walls of the large intestine inhibits the ability to effectively pass stool. The loss of functioning nerve cells prevents peristalsis from moving the stool towards the rectum creating blockages of stool in the large intestine. This results in constipation, bloating, diarrhea, and vomiting, these symptoms if left unchecked can be lethal in infants, and lead to many long term problems in older children. Recorded evidence of Hirschsprung disease dates back to 1691 with

Patients with other abdominal anomalies may have an increased risk for intestinal atresia. For example, children with gastroschisis may also have intestinal atresia, and they should be examined for it (Bauman & Nanagas, 2015). The authors described a case of a neonatal child who was immediately diagnosed and treated for gastroschisis. However, the patient never had a bowel movement after surgical correction. By the fourth week without a bowel movement, an exploratory laparotomy was performed, and the child was diagnosed with intestinal atresia. Unfortunately, about 8 centimeters of small bowel was resected due to ill-appearance, but bowel to bowel anastomosis was performed. Interestingly, the patient still did not have a bowel movement, and

In addition, when the anorectum has not been in the right position during fetal development, defective sensation in the anal canal can be predicted as sensory connections to the CNS cannot be expected to be intact. Fecal continence will also be influenced by the fact that the voluntary striated muscles, represented by the levator muscle, muscle complex and external sphincter, are commonly underdeveloped and cannot function normally. All these congenital problems in ARM patients contribute to their incontinence, especially early in life. A concomitant neurospinal dysraphism will exacerbate dysfunction of the pelvic floor. (Borg, 2013)

According to the Encyclopædia Britannica (2014), a neural tube defect is “any congenital defect of the brain and spinal cord as a result of abnormal development of the neural tube.” This birth defect is “the most common congenital defect of the central nervous system, affecting the brain and/or spinal cord of 300,000 newborns worldwide each year” (Ricks et al., 2012, p. 391). The exact cause of these central nervous system defects is unknown, but there are many contributing factors that are evidenced to assist in the prevention of such a disorder. I will examine the varying types of neural tube defect, populations in which this defect is most prevalent, possible causes of the defect, and how this defect affects the healthcare system.

I’m doing my report on Reglan. Reglan is a medication they give to people with digestion and indigestion problems such as Gastroparesis. What’s Gastroparesis? Gastroparesis is a partial paralysis of the stomach which results in delayed emptying. The reasoning of why I chose Reglan is, because they prescribe it to people that have Gastroparesis, and my niece was diagnosed with it at age of 12 weeks old.

Choice “C” is the best answer. Gastrinomas may occur as single tumors or as multiple, small tumors. About one-half to two-thirds of single gastrinomas are malignant tumors that most commonly spread to the liver and lymph nodes near the pancreas and small bowel.

GERD is relaxation or incompetence of the lower esophagus persisting beyond the newborn period. Relaxation of the

Gastrointestinal presentations which include: failure to thrive leading to poor growth and development in children, steatorrhea leading to frequent greasy and bulky stools, pancreatic manifestations such as pancreatic insufficiency, recurrent acute pancreatitis and chronic pancreatitis, intestinal defects like meconium ileus, distal intestinal obstruction syndrome and rectal prolapse and hepatic problems like prolonged neonatal jaundice (Kumar et al