Sometimes the birth of a child overshadows the doctors delivered the diagnosis – “syndrome Sturge-Weber-Krabbe”. This is a rare congenital angiomatous lesions of the eyes, skin and cerebral membranes. This disease occurs in one person in 100 thousand. For the first time this syndrome has been described by Sturge in 1879, and in 1922, Weber described the signs identified when performing x-rays.
Crabbe in 1934 made the assumption that along with angiomas of the skin, the patient suffers from an angiomatosis of the cerebral membranes. Try to find out what constitutes a syndrome Sturge-Weber-Krabbe, the causes, the symptoms of this disease.
This syndrome is a congenital angiomatosis, ie excessive growth of blood vessels. Pathology affects the Central nervous system, eyes, skin. Syndrome of Weber, a large number of congenital angioma of the face, glaucoma, epilepsy, mental retardation, other ophthalmological and neurological symptoms.
The disease is Diagnosed using radiography of the skull, an MRI or CT scan of cerebral structures, intraocular pressure measuring, ophthalmoscopy, ultrasound of the eye, gonioscopy. Treatment consists of anti-epileptic and symptomatic therapy, and glaucoma is eliminated by conservative and surgical means. In most cases, the prognosis is poor.
Weber Syndrome occurs because of a violation of embryonic development, resulting in two damaged germ layer: ectoderm and mesoderm. It is because of them after a while begins to develop a nervous system, skin, blood vessels and internal organs.
The Reasons for this failure may be the following:
If a person is diagnosed with the syndrome of Weber, the symptoms of this pathology may be different. The main of them – angiomatosis of the skin. This is a vascular stain in all patients is congenital, and over time it begins to increase in size. Mostly located in the cheeks and under the eyes, and when pressed starts to fade. In the beginning, the stain is pink, then gets cherry red or bright red color.
Recommended
A tablet from worms – the relevance of the application for the person
How relevant today, drugs against worms in humans? What kind of creatures these worms, what are modern methods of treatment? We will try to answer these questions, since ignorance in this area is undesirable. Imagine a mummy, which is misleading in k...
What to do if you cracked skin on hands?
Each of us at least once in a lifetime encounter with a small, but very, when the crack the skin on the hands. At this time there are wounds of different sizes, which hurt and cause inconvenience, especially when in contact with water or detergents. ...
Spray Macho man - the key to a proper relationship between the two spouses
Male impotence is a pathological condition associated with abnormal physiological capacity of the penis to reginout and bring sexual partner pleasure in bed.sex impotenceimpotence may not men to pass unnoticed – it usually spoils his nervous sy...
Angiomas can vary in appearance and prevalence, and represent as small scattered pockets, and one big spot, merging together. Angiomatosis is able to cover the throat, the nasal cavity and mouth. In most cases (70%) growth of vessels is unilateral and a 40% change on the face are usually combined with angioma of the limbs and trunk. There may be other dermatological symptoms: swelling of the soft tissues, congenital hemangioma, nevi.
If there is suspicion of the syndrome of Weber, neurology manifested lesion of cranial nerves, resulting in motor and sensory disorders on the opposite the pathological focus side of the body.
In 85% of cases in children the first year of life observed encephalotrigeminal angiomatosis with convulsive syndrome, manifested by epileptic seizures, Jacksonian type, in which the limbs are covered by the cramps. Epilepsy often leads to mental retardation, delayed mental development, in some cases, there may be idiocy, hydrocephalus.
The part of the organs of vision are observed angioma choroid, hemianopsia, heterochromia of the iris, colobomas. In one third of patients diagnosed with glaucoma causing corneal opacity.
The Syndrome of This disease is diagnosed in conjunction with a neurologist, ophthalmologist, and dermatologist epileptology.
The Doctor, analyzing the history of the disease and the patient's complaints, clarifies the age when I first showed signs of illness. Using the neurological examination to assess the skin sensitivity and muscle strength of the extremities of the body.
Skull x-ray detects areas of calcification of the cortex, with dual circuits. Computed tomography of the brain is able to visualize a much larger area. Using MRI to reveal areas of thinning of the cortex, degeneration and atrophy of the cerebral substance, excluding intracerebral tumors, cerebral cyst.
Electroencephalography determines the degree of bioelectrical activity of the brain and sets epiactivity. Eye examination is to check visual acuity, intraocular pressure measurement, conducting perimetry, gonioscopy, ophthalmoscopy, AV-scan ultrasound biometry the eye.
Quite often the patient is sent for consultation to medical genetics.
If diagnosed the syndrome of Weber, the treatment should be only symptomatic. This means that the patient rid of such manifestations of the disease, which worsen his life, as effective treatment is not currentlyexists.
Therapy is as follows:
If you are in the cranial cavity angiomas seriously affect the functioning of the body, the surgery to remove them.
Sadly, this disease, as Weber syndrome has a poor prognosis. You may experience the following complications:
Any preventive measures that can help prevent the development of this disease, do not exist, as the precise causes of the pathology are still not identified.
Thus, the syndrome of Weber – very dangerous congenital disease. Newborns first develop normally, but at the end of the first year of life there are recurrent seizures. Often there is a lag in the development of the limbs, and after some time there is mental retardation. This disease is incurable, you can only make the drugs, not allowing it to deteriorate health.
Article in other languages:
AR: https://tostpost.com/ar/health/14628-krabbe.html
HI: https://tostpost.com/hi/health/14649-krabbe.html
Alin Trodden - author of the article, editor
"Hi, I'm Alin Trodden. I write texts, read books, and look for impressions. And I'm not bad at telling you about it. I am always happy to participate in interesting projects."
Related News
Laxative "Duphalac". The reviews about the drug
the Problem of constipation bothers many, among them not only adults but very young children. Which tool to use, not to hurt the body? Let's look at the drug “Duphalac" of the reviews and applications. the Drug “D...
a Disabled person is a person, restricted in the implementation of the activity for health reasons. The decree of the RF Government No. 95 of 2006 identified three categories that are associated with each other, and which can allo...
"Panadol" (syrup): instructions for use, price, reviews
young children in various diseases need special medicines not only in dosage. Some drugs are tough to swallow kids because of their unpleasant taste. Therefore, the pharmaceutical industry has long been produced by the medicines s...
Drops "Alkospas". Reviews and features of the application
If you believe the statistics, more than 40% of the adult population suffer from alcohol dependence. The patient faces problems in his personal life, risk losing their jobs and friends. In addition, alcohol adversely affects the h...
Pomelo during pregnancy: harm or benefit
Very common exotic citrus fruit is the pomelo. Its homeland is China. In appearance it resembles a huge grapefruit, with the taste of pomelo is much nicer to his brother, and beneficial properties easily compete with him. Anyone i...
Food Allergy in children: causes, characteristics and treatments
Food Allergy in children – the body's response to it is a normal food or any of the ingredients contained in them. Note that the presence of this disease is quite a serious problem for the health of your baby, so you need ti...
Comments (0)
This article has no comment, be the first!