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Results 1 - 10 of 19 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. ... 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). ...
  4. 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. ...
  5. ... and second pharyngeal arch syndromes Goldenhar syndrome Goldenhar-Gorlin syndrome Hemifacial microsomia HFM Lateral facial dysplasia OAV complex ...
  6. ... PORCN gene from a parent. Goltz syndrome Goltz-Gorlin syndrome Genetic Testing Registry: Focal dermal hypoplasia Focal dermal ...
  7. Oral-facial-digital syndrome is actually a group of related conditions that affect the development of the oral cavity (the mouth and teeth), facial features, ...
  8. ... amaurosis, X-linked juvenile retinoschisis, Senior-Løken syndrome, Gorlin-Chaudhry-Moss syndrome, Down syndrome, and fragile X syndrome. Farsightedness is ...
  9. ... Rare Disorders (NORD) MICROPHTHALMIA, SYNDROMIC 2; MCOPS2 PubMed Gorlin RJ, Marashi AH, Obwegeser HL. Oculo-facio-cardio-dental (OFCD) syndrome. Am J Med Genet. 1996 May 3;63( ...
  10. ... Brooks S, Kassner G, Qazi Q, Keogh MJ, Gorlin RJ. Osteoglophonic dysplasia: review and further delineation of the syndrome. Am J Med Genet. 1996 Dec 11;66( ...
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