Cri Du Chat Syndrome Research Paper

400 Words1 Page
bulb-icon

Recommended: Cri du chats syndrome

CRI DU CHAT SYNDROME
Cri du chat syndrome - also known as 5p- syndrome and cat cry syndrome - is erratic genetic condition that is caused by obliteration of genetic material on the small arm (the p arm) of chromosome five. The reason of this erratic chromosomal deletion is unfamiliar.
The symptoms of cri du chat syndrome diverge between people. The unpredictability of the medical symptoms and growing delays may be linked to the magnitude of the deletion of the 5p arm. The scientific symptoms of cri du chat syndrome frequently contain a high-pitched cat-like cry, psychological retardation, late development, characteristic facial structures, small head size (microcephaly), widely-spaced eyes (hypertelorism), low birth weight and weak muscle tone

Show More
Related

  • Bob Probert CTE Report

    642 Words  | 2 Pages

    Bob Probert was a 45 year old man with 4 kids and a wife when he passed away from CTE. He drank, did drugs, and was a womanizer but he didn’t want his kids to find out. He knew they eventually would though and he said that when they did find out, he wanted it to be “straight from the source” (1.). He used to snort cocaine. Once when he was caught while smuggling drugs over the Detroit-Windsor border, he dumped it in the toilet. The first time he tried cocaine was in 1983. It was post-game and before long he was buying an ounce a week which was $800 so it was about $42,000 a year. His work permit was revoked by the US government. He met his wife in Relax Plaza in Windsor and even after he was caught on the border she still stayed with him. To pass drug tests, he would microwave his urine so it would come up clean.

    Read More

  • Rett Syndrome Research Paper

    865 Words  | 2 Pages

    It is characterized by normal early growth and development followed by a slowing of development, the loss of purposeful use of the hands, slowed brain and head growth, problems with walking, seizures, and intellectual disability.

    Read More

  • Canavan Disease Essay

    773 Words  | 2 Pages

    Canavan disease first begins to appear in infants within the first few months of life. Between ages three to five problems with development, controlling head movement, and sitting without support begin to appear. Delay in motor skills also show. These symptoms are caused by the la...

    Read More

  • The Reasoning behind ADHD Awareness Week

    581 Words  | 2 Pages

    As a child growning up, a lot of you may have had these certain condition. I think these the the normal conditions of a child in general. All children may not experience these certain condition at the same time in life, but I am sure nearly all ch...

    Read More

  • Deletion

    1025 Words  | 3 Pages

    The prevalence of this syndrome is estimated to be 1 in 50,000 births [7] with a female to male ratio of 2:1[8].

    Read More

  • FAS Case Study

    958 Words  | 2 Pages

    The fetus in utero may show signs of slow growth and organs may not develop correctly. After birth there can be physical defects evidenced by a smooth skin surface between upper lip and nose, the nose may be upturned, wide set eyes and an extremely thin upper lip. The head may be small in circumference and brain size, deformities of the joints, vision and hearing problems, heart defects and problems with bones and kidneys. There may be problems with the central nervous system and brain, including poor memory and judgement, learning disorders, delayed development, poor coordination and/or balance and hyperactivity or jitteriness, and mood swings. Children born with FAS may have difficulty is school, have poor social skills, have trouble adapting to change, lack impulse control, unable to stay on task and find it hard to plan or work towards a goal. The severity and negative effects range from subtle to serious, they are always

    Read More

  • 5 Senses Vs Mechanical Sense Essay

    399 Words  | 1 Pages

    Neurologically, the amygdala (which associate emotions to recognized faces) might be affected. The neural disconnection creates in the patient a sense that the face he/she is observing is not the face of the person to whom it belongs. Therefore, that face lacks the familiarity and recognition usually associated with it, which results in “derealization” and disconnection from the environment. If the patient sees his/her own face, he/she might perceive no association between the face and his/her sense of “Self”. Medicine indicates that Cotard's syndrome is associated with lesions in the parietal lobe and brain atrophy, especially of the median frontal

    Read More

  • Turner syndrome

    1109 Words  | 3 Pages

    Girls with this syndrome may have many middle ear infections during childhood; if not treated, these chronic infections could cause hearing loss. Up to the age of about 2 years, growth in height is approximately normal, but then it lags behind that of other girls. Greatly reduced growth in height of a female child should lead to a chromosome test if no diagnosis has already been made. Early diagnosis is very importance in order to be able to give enough correct information to the parents, and gradually to the child herself, so that she has the best possibilities for development. Early diagnosis is also important in case surgical treatment of the congenital heart defect (seen in about 20 per cent of cases) is indicated.

    Read More

  • Essay On Angelman Syndrome

    1597 Words  | 4 Pages

    Angelman syndrome has symptoms that can be easily mistaken for cerebral palsy or autism. Symptoms of the disorder include developmental delay, lack of speech, seizures, walking and balance disorders, sleep disturbances, hyperactivity, and frequent laughter or smiling. If a baby or child is diagnosed with Angelman syndrome, they will require life-long care due to the fact that there is no cure. Due to having similarities with autism and cerebral palsy, Angelman syndrome is often misdiagnosed. Misdiagnoses are a prevalent problem today, which can also lead to late diagnoses as well.

    Read More

  • Language Development in Individuals with Down Syndrome

    2336 Words  | 5 Pages

    Some characteristics of DS are: deep folds at the corners of the eyes, hypotonia, short stature, flexible joints, small oral cavity and heart defects (Taylor, Richards, & Brady, 2005). Most individuals with DS have a moderate intellectual disability, although there is a range of disability, from severe to high functioning (IQ above 70). Since DS is a birth defect and not a disease, there are no treatment options. Improvement can be made through physicians, special education, physical therapy, speech therapy, occupational therapy, and psychol...

    Read More

  • Pregnancy and the Dangers of Fetal Alcohol Syndrome

    1545 Words  | 4 Pages

    Possible FAS Symptoms: Growth deficiencies: small body size and weight, slower than normal development and failure to catch up.

    Read More

  • Developmental Coordination Disorder

    1166 Words  | 3 Pages

    The neurological disorder is generally diagnosed in children aged between six and twelve years, the condition affecting boys three times more often than girls (Hamilton, 2002; Gardner, 2008). Despite the fact that DCD affects roughly 6.4 percent of children, few individuals are familiar with the condition (Hamilton, 2002). In fact, a study by Kirby, Davies, & Bryant (2005) revealed that only 54.3% of teachers and 26.7% of general practitioners could accurately define DCD (p. 124). In response, the condition will be briefly outlined here.

    Read More

  • Co-Occurring Disorders Research Paper

    88 Words  | 1 Pages

    I do agree with the co-occurring disorders can be hard to diagnosis because of the symptoms. The consequences in your post does describe many of the women in our homeless shelter. They exhibit dual mental health disorders and have been untreated for many years. The sad thing about those ladies you can’t get them to realize something is not right within their thinking process and behavior. The best thing about it help is being given and their path to self-sufficient and well-being is now a reality. Good

    Read More

  • Fetal Alcohol Syndrome Research Paper

    564 Words  | 2 Pages

    Craniofacial deformities reveal eyes that are small with large inner epicanthic folds. The bridge of the nose is poorly developed. The ears are sometimes large and under developed. When baby is delivered, they may show signs of alcohol withdrawal, depending on the mother’s level of alcohol intake, with signs of delirium tremens. They are inconsolable, display weak grasps, and have difficulty in feeding/sucking.

    Read More

  • Corpus Callosum

    70 Words  | 1 Pages

    The most extreme form of developmental malformation of the corpus callosum is agenesis (Paul, 2007). Agenesis of the corpus callosum (AgCC), which includes not only partial but complete absence of the callosal (Paul, 2011). This occurs due to the disruption of the early stages of the fetal callosal development. This abnormality can be diagnosed in the current ages as visualized through the advanced methods of neuroimaging, MRI or CT scan.

    Read More

More about Cri Du Chat Syndrome Research Paper

Open Document