نتایج جستجو برای: basal cell nevus syndrome

تعداد نتایج: 2291746  

Journal: :journal of dentistry, tehran university of medical sciences 0
ar. bartake assistant professor, department of oral pathology, sinhgad dental college and hospital, pune, india ng. shreekanth assistant professor, department of oral pathology, a.j. institute of dental sciences, mangalore, ind prabhu reader, department of oral and maxillofacial pathology, sdm college of dental sciences and hospital, k. gopalkrishnan professor, department of oral and maxillofacial surgery, sdm college of dental sciences and hospital

odontogenic keratocysts (okcs) are one of the most frequent features of nevoid basal cell carcinoma syndrome (nbs). it is linked with mutation in the ptch gene. partial expression of the gene may result in occurrence of only multiple recurring okc. our patient presented with nine cysts with multiple recurrences over a period of 11 years without any other manifestation of the syndrome.

Journal: :iranian journal of radiology 0
adam domonkos tarnoki department of radiology and oncotherapy, semmelweis university, budapest, hungary; department of radiology and oncotherapy, semmelweis university, budapest, hungary. tel/fax: +36306401183 david laszlo tarnoki department of radiology and oncotherapy, semmelweis university, budapest, hungary katalin klara kiss department of radiology and oncotherapy, semmelweis university, budapest, hungary pal bata department of radiology and oncotherapy, semmelweis university, budapest, hungary kinga karlinger department of radiology and oncotherapy, semmelweis university, budapest, hungary andras banvolgyi department of dermatology, venerology and skin oncology, semmelweis university, budapest, hungary

gorlin-goltz syndrome (ggs) consists of ectodermal and mesodermal abnormalities. in this case report we will investigate lower extremity lesions of ggs. a 52-year-old man with ggs underwent skull and lower extremity computer tomography. radiographic findings included cervical spondylosis, transparent areas with slurred margins, and cerebral falx calcification. tibial and fibular specific cortic...

Journal: :American Journal of Roentgenology 1968

Journal: :The Journal of investigative dermatology 1998
M Aszterbaum A Rothman R L Johnson M Fisher J Xie J M Bonifas X Zhang M P Scott E H Epstein

Mutations in PATCHED (PTC), the human homolog of the Drosophila patched gene, have been identified in most exons of the gene in patients with the basal cell nevus syndrome and in sporadic basal cell carcinomas. We have screened the 23 PTC exons for mutations using single strand conformation polymorphism analysis of DNA from 86 basal cell nevus syndrome probands, 26 sporadic basal cell carcinoma...

Journal: :middle east journal of rehabilitation and health studies 0
sayed mohammad razavi dental implants research center, department of oral and maxillofacial pathology, isfahan university of medical sciences, isfahan, ir iran amir hossein shakibamehr department of prosthodontics, school of dentistry, alborz university of medical sciences, karaj, ir iran saeedeh khalesi dental research journal, department of oral and maxillofacial pathology, school of dentistry, isfahan university of medical sciences, isfahan, ir iran; department of oral and maxillofacial pathology, school of dentistry, isfahan university of medical sciences, isfahan, ir iran. tel: +98-3117922879; +98-9131079487, fax: +98-3116687080

nevoid basal cell carcinoma syndrome (bcns) is an autosomal dominant inherited disorder. multiple organ systems may be affected in this syndrome including abnormalities of the skin, skeletal system, genitourinary system and central nevus system. in this report, we present a case of nevoid basal cell carcinoma syndrome in a 26-year-old male patient. the patient had multiple odontogenic keratocys...

Journal: :Dermatology online journal 2007
David N Lortscher Roberta D Sengelmann Shawn B Allen

Basal cell nevus syndrome is an autosomal dominant disorder characterized by multiple basal cell carcinomas, along with numerous other documented clinical features. Acrochordons (or skin tags) are common benign neoplasms that are appropriately left untreated in most patients. We describe two patients with known BCNS who were found to have multiple BCCs that clinically resembled acrochordons. Ou...

Journal: :Science 1997
A E Oro K M Higgins Z Hu J M Bonifas E H Epstein M P Scott

Mutations in the tumor suppressor gene PATCHED (PTC) are found in human patients with the basal cell nevus syndrome, a disease causing developmental defects and tumors, including basal cell carcinomas. Gene regulatory relationships defined in the fruit fly Drosophila suggest that overproduction of Sonic hedgehog (SHH), the ligand for PTC, will mimic loss of ptc function. It is shown here that t...

Journal: :Nihon Koku Geka Gakkai zasshi 1976
T Ohtani H Fukuda T Funakoshi S Mogi M Kojima

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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