منابع مشابه
Neurocutaneous syndromes and epilepsy-issues in diagnosis and management.
Epilepsy may be seen as a feature of many of the neurocutaneous syndromes. The challenge lies within the diagnosis of the specific disorder and ultimately control of the epilepsy. Tuberous sclerosis is the most common of the disorders with a frequency of 4.9/100,000. An autosomal-dominant condition, diagnostic features may be unclear under 2 years of age. Population studies suggest a prevalence...
متن کاملCommon Neurocutaneous Syndromes.
Neurocutaneous syndromes are a diverse group of neurologic disorders with concurrent skin manifestations. Most neurocutaneous syndromes have a genetic basis and are believed to arise from a defect in the differentiation of the primitive ectoderm. In this regard, the skin can be a window into the central nervous system and can aid in the diagnosis of neurologic disease in children. The cutaneous...
متن کاملNeurocutaneous syndromes and retroperitoneal tumors.
A patient with multiple basal cell carcinoma syndrome, a symptom complex characteristized by nevoid basal cell carcinomas of the skin, jaw cysts, skeletal abnormalities, and hyporesponsiveness to parathormone is presented. In addition, the patient had a retroperitoneal lymphagiomyoma, a hamartomatous lesion, causing ureteral obstruction. The association of neuroectodermic syndromes and retroper...
متن کاملNeurocutaneous melanosis and epilepsy surgery
To the Editor: Dr Jean Latrelle, an eminent Parisian neurologist at the time of a meeting in Harriman, N.Y., started his discussion by saying, “Everything has been written, but not everything has been read”. I found the description of a patient with neurocutaneous melanosis by Oliveira de Andrade et al. (Epileptic Disord, 2004; 6: 145-52) interesting. For the past 30 years we have been followin...
متن کاملNeuro-ophthalmic features of the neurocutaneous syndromes.
This review highlights the diagnostic criteria and neuro-ophthalmic symptoms and signs of the more commonly seen neurocutaneous disorders, including NF1 and NF2, tuberous sclerosis, VHL disease, Sturge-Weber disease, and AT. The distinct neuro-ophthalmic features in each of these hereditary and congenital disorders play an important role in clinical diagnosis.
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Journal of the Turkish Epilepsi Society
سال: 2016
ISSN: 1300-7157
DOI: 10.5505/epilepsi.2016.63634