Epilepsy and migraine in a patient with Urbach–Wiethe disease
نویسندگان
چکیده
We report the clinical, neuroradiological, and molecular genetic findings in a patient with lipoid proteinosis or Urbach-Wiethe disease. Interestingly, in this patient epilepsy and migraine were the symptoms leading to the diagnosis of the disease, contrary to most patients in whom skin abnormalities are the first recognized symptoms.
منابع مشابه
Lipoid proteninosis:case report
URBACH-WIETHE is a very rare autosomally recessive disorder characterized by infiltration of hyaline material into skin,oral cavity,larynx,and internal organs.in this report we persent a case of a 22 year old woman with small scars on her face,hoarseness,firm tongue and beaded papules along the margins of eyelids,who was referred to the deparment of ophthalmology of Kerman university No3: hospi...
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ورودعنوان ژورنال:
- Seizure
دوره 16 شماره
صفحات -
تاریخ انتشار 2007