Epilepsy associated tuberous sclerosis; a case report from Bangladesh

被引：1

作者：

Shrestha, Abhigan Babu ^{[1
]}

Shrestha, Sajina ^{[2
]}

Seemanta, Senjuti ^{[1
]}

Pokharel, Pashupati ^{[3
]}

Alam, Waqar ^{[1
]}

机构：

[1] M Abdur Rahim Med Coll, Dept Internal Med, Dinajpur, Bangladesh

[2] KIST Med Coll, Dept Internal Med, Imadol, Patan, Nepal

[3] Dept Internal Med, Maharajgunj Med Campus, Kathmandu, Nepal

来源：

ANNALS OF MEDICINE AND SURGERY | 2022年 / 78卷

关键词：

Angiofibroma; Epilepsy; Case report; MRI; Subependymal nodules; Tuberous sclerosis complex; FACIAL ANGIOFIBROMAS; TSC1-TSC2; COMPLEX;

D O I：

10.1016/j.amsu.2022.103738

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Tuberous sclerosis or Bourneville's disease is a rare autosomal dominant disease affecting many organs like the brain, heart, lungs, eyes, kidneys and skin. It is characterized by neurological manifestation like epilepsy, cutaneous changes and the formation of benign lesions in multiple organs. The symptoms are apparent only in late childhood, which limits the early diagnosis in infancy. Here, we report a case of a 15 year old female child with tuberous sclerosis.

引用

页数：5

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