Content

»Genodermatoses
»X-Linked Recessive
»X-Linked Dominant
»Syndromes with Defective DNA Repair
»Xeroderma Pigmentosum
»Cockayne Syndrome
»Trichothiodystrophy
»Bloom Syndrome
»Rothmund–Thomson Syndrome
»Dyskeratosis Congenita
»Ataxia-Telangiectasia Syndrome
»Fanconi Syndrome
»Syndromes of Tumor Suppression
»Basal Cell Nevus Syndrome (Gorlin Syndrome)
»Neurofibromatosis, Type I (Von Recklinghausen Disease)
»Neurofibromatosis, Type II (Bilateral Acoustic NF)
»Carney Syndrome (NAME or LAMB Syndrome)
»Muir–Torre Syndrome
»Tuberous Sclerosis
»Cowden Syndrome (Multiple Hamartoma Syndrome)
»Multiple Endocrine Neoplasia (MEN)
»Bannayan–Riley–Ruvalcaba Syndrome
»LEOPARD Syndrome (Multiple Lentigines Syndrome)
»Peutz–Jeghers Syndrome
»Gardner Syndrome
»Birt–Hogg–Dubé Syndrome
»Dysplastic Nevus Syndrome

 
 
 

Gardner Syndrome

  • AD, APC gene encoding tumor suppressor gene (ras proto-oncogene)
  • Cutaneous epidermoid cysts, osteomas (mandible, maxilla), supernumerary teeth, odontomas, fibromas, congenital hypertrophy of the retinal pigment epithelium (CHRPE)
  • Tumors: GI adenocarcinoma (inevitable), osteochondromas, thyroid papillary carcinoma, hepatoblastoma, adrenal adenomas
   
 
Gardner – birds CHiRP in the GARDen
 
   





 
 
 

 

 

 

 

 

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