Information on Kearns Sayre Syndrome

Posted on 26th | Posted by admin in Health

KSS is characterized by progressive limitation of eye movements until there is complete immobility, accompanied by eyelid droop. It is also related with abnormal accumulation of pigmented material on the membrane lining the eyes.

Kearns-Sayre Syndrome belongs (in part) to a group of rare neuromuscular disorders known as mitochondrial encephalomyopathies. Kearns-Sayre Syndrome (KSS) is a very uncommon fatal multisystem disorder which generally affects female and males before the age of 20, and it is characterized by progressive outer ophthalmoplegia, gentle skeletal muscle weakness, retinal pigmentation, left bundle branch block or intracardiac conduction blemish. It is the cause of abnormalities in the DNA of mitochondria - small rod-like structures found in every cell of the body that produce the power that drives cellular functions.

Detailed Information on Megalencephaly

Posted on 16th | Posted by admin in Health

Megalencephaly is a type of cephalic disorder and also called macrencephaly.

Megalencephaly is marked by an abnormally large, heavy, usually malfunctioning brain. The head may be enlarged at birth or become abnormally big in the early years. The brain weight is greater than standard for the age and sex of the baby or child. This results in a large, often asymmetrical head. Head enlargement may be evident at birth or the head may become abnormally large in the early years of life. Symptoms of megalencephaly may include delayed development, convulsive disorders, corticospinal (brain cortex and spinal cord) dysfunction, and seizures.

Information on Laron Syndrome

Posted on 4th | Posted by admin in Health

Laron Syndrome is an uncommon genetic disease that causes humans to be short.

Laron syndrome type I (LTD1) a rare genetic disorder. Laron syndrome is caused by the body’s inability to use the growth hormone (GH) that it produces. Laron syndrome type I (LTD1) causes short stature. People with this disease lack certain receptors that are important to human growth. Laron Syndrome is normally developed shortly after birth.  Laron Syndrome occurs more often in girls than boys.  Also, people with the disease usually have deep-set eyes, smaller hands and feet, and a high pitched voice.

Complete Information on Eagle’s Syndrome

Posted on 19th | Posted by admin in Women

Eagle syndrome can occur unilaterally or bilaterally and most oftenly results in symptoms of dysphagia, headache, pain on gyration of the neck, pain on extension of the tongue, change in voice, and a sensation of hypersalivation.

Eagle syndrome is medically name as the elongation of the styloid method and stylohyoid ligament calcification. Eagle syndrome is an accumulate of symptoms caused by an elongated ossified styloid process. This typically occurs with aging, and frequently results in sharp, irregular pain along the glossopharyngeal nerve that is found in the hypopharynx and at the base of the tongue.

Complete Information on Choroid plexus papillomas

Posted on 5th | Posted by admin in Health

Choroid plexus carcinoma is an uncommon, cancerous kind of this tumor. It is not treated with operation only, but requires extra therapy including chemotherapy and sometimes radioactivity therapy. Hydrocephalus may remain and is managed by CSF shunting.

Choroid plexus papillomas are one of the most common tumors of the nervous system in infants. The most frequent early symptoms, megalocephalia and vomiting, caused by elevated intracranial pressure often lead to a diagnosis only at a critical clinical stage. CPPs are commonly observed in the lateral ventricles of children, but they can be encountered in adults. While the vast majority of these neoplasms are benign, a small percentage can be malignant.CPPs arise from the single layer of cuboidal epithelial cells lining the papillae of the choroid plexus. The choroid plexus is associated with the ventricular lining of the body and trigone.