Diagnostic parameters of children with basal cell carcinoma nevus syndrome

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Basal Cell Nevus Syndrome Showing Several Histologic Types of Basal Cell Carcinoma

Basal cell nevus syndrome (BCNS), or Gorlin Syndrome, is an autosomal dominant disorder, characterized by multiple developmental abnormalities and associated with germline mutations in the PTCH gene. Patients show multiple and early onset basal cell carcinomas (BCCs) in skin, odontogeniccysts in the jaw, pits on palms and soles, medulloblastoma, hypertelorism, and calcification of the falx cere...

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Retraction: Basal Cell Nevus Syndrome Showing Several Histologic Types of Basal Cell Carcinoma

On September 30, 2011, Annals of Dermatology in Volume 23, Number Supplementary 1, published a case report by Go JW, et al. on the basal cell nevus syndrome. We accepted the article after having been informed in writing, by the authors, that it had not been submitted for publication elsewhere. In fact, however, the same case had already been reported by Moon MS, et al., the colleagues in the sa...

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[A case of basal cell nevus syndrome].

A case of basal cell nevus syndrome is reported. The patient, a 25-year-old man, had no family history of this condition. The patient showed multiple mandibular cysts, calcification of the falx cerebri, bridging of the sella turcica, ocular hypertelorimsm, a broad nasal root, and pitting of the palms. These findings correlate with reports in the literature and permitted the diagnosis of basal c...

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Meningeal calcification in basal cell nevus syndrome.

To cite: Nair PP, Khilari M, Peddawad D, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2013200545 DESCRIPTION A 20-year-old woman presented with history of headache for 1 year. The headaches were mild to moderate in intensity, bilateral and non-throbbing, with no symptoms suggestive of raised intracranial pressure. The patient had hyperpigmented skin lesi...

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Basal cell nevus syndrome. A case report.

An 11-year-old boy with multiple dentigerous cysts in the maxilla and mandible is described. Other findings seen in the face, plantar skin, skeletal system and oral cavity indicated the lesions to be due to the basal cell nevus syndrome. This was further confirmed by the presence of similar abnormalities in his father and brother.

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ژورنال

عنوان ژورنال: Dermatology Online Journal

سال: 2016

ISSN: 1087-2108

DOI: 10.5070/d3229032536