ANGIOMATOSE DE STURGE WEBER PDF

Sturge — beschrieben. Augenerkrankungen z. Im Computertomogramm sieht man den Gewebsschwund im Gehirn Hirn atrophie. In der Regel ist eine Augensymptomatik an der Seite festzustellen, an der das Angiom im Gesicht besteht. Literatur[ Bearbeiten Quelltext bearbeiten ] W.

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The purpose of this paper is to discuss the epidemiological, clinical, paraclinical and therapeutic aspects of the disease while emphasizing the importance of early diagnosis. Results: We reported a study of 6 children, 3 boys and 3 girls.

Their ages ranged from 3 months to 10 years with a mean age of 3 years and a half. The plane facial angioma occupying the territory of V1 was noted in 5 patients. Five patients had partial seizures contralateral to the cutaneous angioma, while only one patient had generalized tonic-clonic seizures. Psychomotor regression was observed in 2 cases. Ophthalmologic examination showed congenital glaucoma in 2 patients and signs of visual impairment in a patient.

Brain imaging performed in all patients was in favor of SWS. The electroencephalogram EEG was pathological in 3 patients. All patients have received antiepileptic drugs associated with multidisciplinary rehabilitation with variable changes depending on the severity of the disease and earliness of care. Facial port-wine stains and Sturge-Weber syndrome. Roach E. Diagnosis and management of neurocutaneous syndromes.

Semin Neurol. Encephalo-angiomatosis in black children. A report of 2 cases. S Afr Med J. The cutaneous manifestations of Sturge-Weber syndrome. J Clin Neuroophthalmol. Prognosis in Sturge-Weber disease: comparison of unihemispheric and bihemispheric involvement. J Child Neurol. Pulmonary haemodynamics in patients with OSAS or an overlap syndrome.

Monaldi Arch Chest Dis. Update on Sturge-Weber syndrome: diagnosis, treatment, quantitative measures, and controversies. Lymphat Res Biol. Neurocutaneous syndromes. Adolesc Med. The incidence of birthmarks in the neonate. Sturge-Weber syndrome in patients with facial port-wine stain.

Pediatr Dermatol. Sturge-Weber syndrome: from the past to the present. Eur J Paediatr Neurol. Sturge-Weber syndrome: study of 55 patients. Can J Neurol Sci. Histopathologic findings in 37 cases of functional hemispherectomy. Ann Diagn Pathol. Sturge-Weber syndrome: clinical spectrum, disease course, and outcome of 30 patients. Neuroradiol ; 19 : - An infantile-onset, severe, yet sporadic seizure pattern is common in Sturge-Weber syndrome. S, SHIN. Klapper J. Headache in Sturge-Weber syndrome.

The phakomatoses. Outcome of Sturge-Weber syndrome in 52 adults. Am J Med Genet. Sturge-Weber syndrome with posterior fossa involvement. ET Al. Syndrome de Sturge Weber Krabbe, forme grave chez une jumelle monozygote.

R Sturge - Weber syndrome. Adoleses Med. Comi A. Presentation, diagnosis, pathophysiology, and treatment of the neurological features of Sturge-Weber syndrome. Prophylactic antiepileptic treatment in Sturge-Weber disease. A pilot study of the modified Atkins diet for Sturge-Weber syndrome. Epilepsy Res. The value of the brain scan and cerebral arteriogram in the Sturge-Weber syndrome. Proc Aust Assoc Neurol. Central nervous system structure and function in Sturge-Weber syndrome: evidence of neurologic and radiologic progression.

ENDOBUTTON SMITH AND NEPHEW PDF

Sturge-Weber-Krabbe-Syndrom

Os sintomas tendem a se estabilizar com o tempo 7. O manejo da SSW envolve o envolvimento multidisciplinar como neurologista, oftalmologista e dermatologista. Update on Sturge-Weber syndrome: diagnosis, treatment, quantitative measures, and controversies. Lymphat Res Biol ;e Sturge-Weber syndrome: a review.

ESCRIMA KATA PDF

Síndrome de Sturge-Weber

The purpose of this paper is to discuss the epidemiological, clinical, paraclinical and therapeutic aspects of the disease while emphasizing the importance of early diagnosis. Results: We reported a study of 6 children, 3 boys and 3 girls. Their ages ranged from 3 months to 10 years with a mean age of 3 years and a half. The plane facial angioma occupying the territory of V1 was noted in 5 patients.

CHUBB ALARME INCENDIE PDF

Het Sturge Weber syndroom

Ook in de hersenen bestaan er hemangiomen van de leptomeningen zachte hersenvliezen , die aanleiding geven tot epilepsie en atrofie. Verder kunnen optreden: ontwikkelingsstoornissen, gezichtsveldstoornissen, en andere neurologische uitval zoals verlammingen. Alle symptomen zijn direct of indirect een gevolg van de abnormale bloedvatontwikkeling. Van het syndroom is sprake als de eerste twee kenmerken aanwezig zijn. Een wijnvlek zonder verdere afwijkingen binnen de schedel valt er niet onder. Soms komen de hersenafwijkingen voor zonder wijnvlek.

FREDERICK BUECHNER WISHFUL THINKING PDF

Syndrome de Sturge-Weber

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