Gorlin syndrome (Q46685): Difference between revisions
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A síndrome de Gorlin, também conhecida como síndrome de carcinoma nevoide de células basais ("naevoid basal cell carcinoma syndrome" - NBCCS), é uma condição hereditária caracterizada por uma ampla gama de anormalidades de desenvolvimento (queratocistos odontogênicos das mandíbulas, hiperceratose palmoplantar, anormalidades esqueléticas, calcificações ectópicas intracranianas e dismorfismo facial) e uma predisposição para desenvolver neoplasias malignas (como carcinomas múltiplos de células basais ou meduloblastoma) e neoplasias benignas nas mandíbulas, coração e ovários. | |||
| description / en | description / en | ||
Gorlin syndrome, also known as naevoid basal cell carcinoma syndrome (NBCCS), is a hereditary condition characterised by a wide range of developmental abnormalities (odontogenic keratocysts of the jaws, hyperkeratosis of palms and soles, skeletal abnormalities, intracranial ectopic calcifications, and facial dysmorphism) and a predisposition to develop malignant neoplasms (such as multiple basal cell carcinomas or medulloblastoma), and benign neoplasms in the jaw, heart, or ovaries. | |||
Revision as of 15:26, 13 August 2026
Gorlin syndrome, also known as naevoid basal cell carcinoma syndrome (NBCCS), is a hereditary condition characterised by a wide range of developmental abnormalities (odontogenic keratocysts of the jaws, hyperkeratosis of palms and soles, skeletal abnormalities, intracranial ectopic calcifications, and facial dysmorphism) and a predisposition to develop malignant neoplasms (such as multiple basal cell carcinomas or medulloblastoma), and benign neoplasms in the jaw, heart, or ovaries.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD2D.4 |
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| English | Gorlin syndrome |
Gorlin syndrome, also known as naevoid basal cell carcinoma syndrome (NBCCS), is a hereditary condition characterised by a wide range of developmental abnormalities (odontogenic keratocysts of the jaws, hyperkeratosis of palms and soles, skeletal abnormalities, intracranial ectopic calcifications, and facial dysmorphism) and a predisposition to develop malignant neoplasms (such as multiple basal cell carcinomas or medulloblastoma), and benign neoplasms in the jaw, heart, or ovaries. |
