Tuberous sclerosis
Hereditary disease characterized by seizures, mental retardation, developmental delay, and skin and ocular lesions. First signs usually occur during infancy or childhood but in rare cases may not occur until 2nd or 3rd decade.
Disease Alternative Name
Topical RapamycinA Novel Approach to Facial Angiofibromas in Tuberous Sclerosis Topical sirolimus seems to be a fairly well tolerated choice in future. After the incidental observation of improvement in angiofibromas in a kidney transplant...
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Child needs evaluation by Pediatric Neurologist/ Neurologist. MRI failed to demonstrate priventricular nodules suggestive of TS. Probable ASD.Needs clinical evaluation. Start speech therapy
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Recent Cases of Tuberous sclerosis
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Top Cases of Tuberous sclerosis
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Dr KUTE HOSPITAL
Dr KUTE HOSPITAL
Govt. Medical College Miraj
D M &S
Trending Cases
What is the treatment of ulcer in angle of both lips again and again? I give tess oint there is recover but it produce again what is cause and treatment?
Dr. Nirmal Shah0 Like1 AnswerA female 36 years, gravida 3 para 2 comes with complaints of headache, loss of sight and is in labour with poor cervical dilatation progress. on admission, the BP is 178/102 with no history of convulsions and magnesium sulphate is given. A LSCS is performed under spinal anesthesia with BP stabilised. she is transferred to ICU for post operative management with BP continuing to increase . After 5 days, a feedback is given that the patient is discharged and gained her sight. What caused the loss of sight?
Dr. Prashant Vedwan1 Like0 Answer
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