Clinical case of manifestation of tuberous sclerosis in a child
We have provided information about prevalence, etiology and pathogenesis of the tuberous sclerosis complex, a rare hereditary disease, caused by genetic mutation in TSC1 and TSC2 genes. Clinical and morphological manifestations of the disease were considered, according to updated diagnostic criteria...
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| Main Authors: | , , , , |
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| Format: | Book |
| Published: |
Zaslavsky O.Yu.,
2021-10-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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