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angiofibroma/kuhara

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NakalaMajaribio ya klinikiHati miliki
2 matokeo

Rare syndromes.

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Ingia / Ingia
Dermatologists may also encounter patients presenting with skin lesions that reflect an underlying endocrine disorder not commonly seen in daily practice. Some of these endocrine disorders include glucagonoma, neurofibromatosis type 1, McCune-Albright syndrome, multiple endocrine neoplasia, the

Effects of rapamycin on angiomyolipomas in patients with tuberous sclerosis.

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Ingia / Ingia
BACKGROUND Tuberous sclerosis (TS) is a systemic disease, with an autosomal dominant pattern of inheritance caused by mutations in two genes (TSC1 and TSC2) that cause tumours (angiomyolipomas [AML], angiofibromas, astrocytomas). Constant and inadequate proliferation occurring in TS may be blocked
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