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Results 1 - 10 of 62 for Gorlin syndrome
  1. Gorlin syndrome, also known as nevoid basal cell carcinoma syndrome, is a condition that affects many areas of the body and increases the risk of developing ...
  2. Meier-Gorlin syndrome is a condition primarily characterized by short stature. It is considered a form of primordial dwarfism because ... a small head size, most people with Meier-Gorlin syndrome have normal intellect.Some people with Meier-Gorlin ...
  3. Epstein EH. Nevoid basal cell carcinoma syndrome (Gorlin syndrome). In: Lebwohl MG, Heymann WR, Coulson IH, Murrell DF, eds. Treatment of Skin Disease: Comprehensive Therapeutic Strategies. 6th ed. Philadelphia, PA: Elsevier; 2022: ...
  4. ... the characteristic features of a genetic condition called Gorlin syndrome.Many individuals with a 9q22.3 microdeletion have ... 3 microdeletions also cause the characteristic features of Gorlin syndrome (also known as nevoid basal cell carcinoma syndrome). ...
  5. Gorlin-Chaudhry-Moss syndrome is a condition that affects many parts of the body. The signs and symptoms of this disorder are apparent from birth or infancy. ...
  6. ... and second pharyngeal arch syndromes Goldenhar syndrome Goldenhar-Gorlin syndrome Hemifacial microsomia HFM Lateral facial dysplasia OAV complex ...
  7. ... PORCN gene from a parent. Goltz syndrome Goltz-Gorlin syndrome Genetic Testing Registry: Focal dermal hypoplasia Focal dermal ...
  8. Risk Factors for Soft Tissue Sarcoma (American Cancer Society)  
    Soft Tissue Sarcoma/Prevention and Risk Factors ... Soft Tissue Sarcoma ... American Cancer Society ... A risk factor is anything that changes your chance of getting ...
  9. ... bone. Mutations in the ORC1 gene cause Meier-Gorlin syndrome, a condition characterized by short stature, underdeveloped kneecaps, ... a reduction in replication licensing leads to Meier-Gorlin syndrome. Researchers speculate that such a reduction delays the ...
  10. ... the PTCH1 gene have been found to cause Gorlin syndrome (also known as nevoid basal cell carcinoma syndrome), ... to form the tumors that are characteristic of Gorlin syndrome. It is less clear how PTCH1 gene mutations ...
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