Sturge-Weber Syndrome Research Paper

Asymmetry of the orbits leads to strabismus [crossed eye] (Craniosynostosis). Intracranial pressure can develop if the baby has Complex Synostosis, and can affect the baby in various ways, like a full or bulging fontanelle [soft spot located on the top of the head], sleepiness [or less alert than usual], increased irritability, poor feeding, projectile vomiting, seizures, bulging eyes, development delays, blindness, eye movement disorders, cognitive impairment [affects memory or thinking skills], or in rare instances, death. The risk of intracranial pressure from simple synostosis is small, as long as the suture and head shape are fixed surgically. Doctors cannot predict which children will develop this pressure problem; however, with more than one suture fused, the likelihood of increased pressure is higher. Surgery is typically the recommended treatment because the physician can reduce the pressure in the head and correct the deformities of the face and skull bones, but some children may not require surgery (Craniosynostosis).

Birthmarks are not uncommon and most of the time they can be caused by genetics. Georgiana's supposed defect, can be just a mere case of bad genetics. In the story we learn that the mark on her face is crimson

The Birthmark is about a Scientist named Aylmer. Aylmer has dedicated his life to his work. His wife, Georgina is a beautiful, undesirable women. Georgina has a little birthmark on her left cheek. The birthmark is her only imperfection. On the first page of the story, it describes that the birthmark is the color of a deeper crimson, and the mark has some similarity to the human hand. Thus takes the nickname, the "Crimson hand". In paragraph eight it tells us that the birthmark is a "symbol of his wife's liability to sin, sorrow, decay, and death". It showed that Georginaʻs impurity was looked down upon or frightened by the community and even her own husband. Because of his wife's birthmark, Aylmer was continuously bothered by itsʻ presence. It bothered him because the

My six year old nephew Jackson suffers from Lennox Gastaut syndrome, a rare form of epilepsy most commonly found in children. This syndrome causes the child affected to experience frequent and varied seizures and it severely affects mental development, thus treatment is very difficult. There is no actual cure for LGS but remedies are available, such as a ketogenic, mostly fat, diet or antiepileptic drugs, but even these are not reliable to remedy seizures. Another such solution is to remove the part of the brain which causes the seizures altogether. When people have seizures, their brain turns

Saethre-Chotzen syndrome is a craniosynostosis which the main clinical feature is the presence of uni/bi-lateral coronal synostosis. Other facial clinical features are strabism, bulgy eyes and small sized ears with a peculiar prominent cus. Patients can also present syndactily of digits with various severities.

The air became thinner and my steps got steeper. Each breath I took I acted as if it was my last

Epilepsy was conceptually defined in 2005 as a disorder of the brain characterised by enduring predisposition to generate epileptic seizures (1). This disorder is approached with such fear and trepidation by the medical and lay person alike, due to it expression of violent muscular activity in most cases. Much work and study has been done to understand that pathological process, and one etiology that is of surgical importance is temporal lobe epilepsy. Although this is not a common cause of epilepsy, it certainly has the potential for a good outcome if managed surgically. In this review the detailed surgical approach and management of this condition will be discussed, with a case presentation to highlight the topic.

Some of the many symptoms include; hair loss, wrinkled skin, stunted growth, heart attack, small and usual facial features, osteoporosis, loss of sight, loss of hearing, dental abnormalities, big head, and joint abnormalities. The cause of the appearance of bulged head too large for the rest of the face is a hallmark of Progeria. One of the reasons why that happens is because the children’s fontanelle with Progeria remains open. Fontanelles are soft spots in a newborns head that are caused by gaps between the plates of the bone in the skull that is supposed to later close together. People with the disease are still able to conceive, but to this day there hasn’t been one to even try.

The first reported case of LS occurred when Denis Archibald Leigh examined a baby boy who displayed symptoms similar to that of Wernicke's, -description of W (new source)-. Before the child passed, he exhibited child: development regression, somnolence, bulbar palsy, spasticity lims. (JNNP)

Birthmarks or birth defects were of the rarest types yet most intriguing cases. In cases in which a deceased person was identified the details of whose life unmistakably matched the child’s statements, a close correspondence was nearly always found between the birthmarks and/or birth defects on the child and the wounds on the deceased person. In 43 of 49 cases in which a medical document (usually a postmortem report) was obtained, it confirmed the correspondence between wounds and birthmarks (or birth defects). Birthmarks is drafted proof that some forms or reincarnation in fact exist. It is said to be a sign of a past life. Fatal wounds (or birth

Sutures in the in skull fuse prematurely causing the patient to have a short, wide head with bulging eyes that are wide-set. The shallow eye sockets cause strabismus (the eyes to point in different directions). Because the skull is wider than normal the patient will have a beak-like nose and an underdeveloped upper jaw. This causes dental problems and can also contribute to hearing loss. In a normally developing individual, the eyes start lower on the head and move upwards as the child grows. With Crouzon patients, this is interrupted and the ear canals can become malformed. The chin will protrude and make the child look as if it has a concave face. The patient may also have a cleft palate or lip.

Marfan Syndrome is a genetic disorder that will affect different parts of the body through the connective tissue. The connective tissue is important because it helps you get strength to move, to have muscles, and lets blood run through your vessels, etc. The part of the body in which is most affected would be the eyes, blood vessels, and also the skeletal regions such as the spine. This can also affect what you can do in life because it can cause breathing complications (Deitz et

What is Crouzon Syndrome? It’s a genetic disorder that is characterized by the premature fusion of certain skull bones(craniosynostosis). When the bones are fused permanently it causes the shape of the head and face to be deformed. I choose this topic because my nephew Karter was born with Crouzon Syndrome it encouraged me to have a better understanding of this disorder. As I mention before fusion prevents the skull from growing normally and will require surgery to be corrected. The Effects of Crouzon syndrome is wide bulging eyes and vision problems which is caused by the shallow eye sockets, the eyes doesn’t point in the same direction (strabismus.) Kids with Crouzon syndrome may have a beaked shaped nose, underdeveloped upper jaw line,

Crouzon syndrome is caused by a mutation in the fibroblast growth factor receptor-2 (FGFR2) gene [2]. Premature craniosynostosis, midface hypoplasia and exophthalmos account for the triad of Crouzon syndrom. Premature closure of cranial sutures, most commonly the coronal and sagittal ones, results in abnormal skull growth, affects the growth and development of the orbits and maxillary complex. Other clinical features include hyperteleorism, exophtalmos, strabismus, beaked nose, short upper lip, maxillary hypoplasia and relative mandibular prognathism. Acanthosis nigricans is the main dermatologic manifestation of Crouzon syndrome Optic atrophy is frequently seen and has been reported 30 to 80% of patients. Increased intracranial pressure leading to optic atrophy may occur, which can produce blindness if the condition is not

Having a baby is a wonderful event and the process is even better. To know that life comes from two people engaging in one activity is mind-blowing. Life then grows inside of a woman for nine months, where the baby is nurtured and breathes life through their mother. Then the mother goes into labor followed by delivery. After delivery, the woman can now hold the baby that grew inside of her. The process of having a baby is very beautiful. There are several aspects and all of them are very different from each other. When I think about it, it’s hard to understand how all of this can happen but that just makes it even more special.