منابع مشابه
Tuberous sclerosis: a case report.
The aim of this case report was to present a typical case of tuberous sclerosis. On 28 April 2012 a 8 year old female student reported as out patient of Ophthalmology Department, BSMMU, Dhaka. After taking history from the patient, ocular and systemic examinations were done. This patient had recurrent attacks of convulsion since 2 months of age and blurring of vision for 3 months. Ocular examin...
متن کاملAssociation of Pemphigus Vulgaris and Tuberous Sclerosis: A case report
Pemphigus vulgaris is a blistering autoimmune disease with suprabasal cleft formation, which is the most common autoimmune blistering disease in eastern countries, such as Middle East. Predisposition to pemphigus is linked to genetic factors. Tuberous sclerosis is also a genetic disorder of hamartoma formation in many organs, particularly the skin, brain, eye, kidney and heart. We report ...
متن کاملTuberous sclerosis: literature review and case report
Tuberous sclerosis (TS) or Bourneville’s disease is a rare, multisystemic genetic disorder. It involves alterations to ectodermal and mesodermal cell differentiation and proliferation, causing benign hamartomatous tumors, neurofibromas and angiofibromas in the brain and other vital organs including the kidney, heart, eyes, lungs, skin and mucosa. It also affects the central nervous system and p...
متن کاملTuberous sclerosis complex: A case report
Tuberous Sclerosis Complex (TSC) was first described in the late 1800s as a relative of neurofibromatosis, but it has since been identified as a discrete disorder. Patients with TSC typically present with facial adenomas, seizure disorder, and a developmental disability. The syndrome is caused by mutations in either chromosomes 9 or 16, both of which code for cell development and maturation. Th...
متن کاملTuberous Sclerosis in a Young Female- A Rare Case Report
Tuberous sclerosis complex Syndrome (TSCs) is an autosomal dominant disorder affecting multiple organs; caused by mutations of either the TSC1 or TSC2 gene encoding hamartin and tuberin respectively. It is characterized by the development of benign tumours affecting different body systems. The most common visible manifestations of TSC are facial angiofibromas and the formation of hamartomas in ...
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ژورنال
عنوان ژورنال: Asian Pacific Journal of Health Sciences
سال: 2019
ISSN: 2350-0964,2349-0659
DOI: 10.21276/apjhs.2019.6.2.17