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Syndrome

Basal Cell Nevus Syndrome

AMW:DIS:040009

Hereditary disorder consisting of multiple basal cell carcinomas, odontogenic keratocysts, and multiple skeletal defects, e.g., frontal and temporoparietal bossing, bifurcated and splayed ribs, kyphoscoliosis, fusion of vertebrae, and cervicothoracic spina bifida. Genetic transmission is autosomal dominant.

Pathology clinical
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Basal Cell Nevus Syndrome has parent Abnormalities, Multiple
Basal Cell Nevus Syndrome has parent Basal Cell Carcinoma
Basal Cell Nevus Syndrome has parent Bone Diseases, Developmental
Basal Cell Nevus Syndrome has parent Neoplastic Syndromes, Hereditary
Basal Cell Nevus Syndrome has parent Odontogenic Cysts

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