Matches in DBpedia 2014 for { <http://dbpedia.org/resource/Crouzonodermoskeletal_syndrome> ?p ?o. }
Showing items 1 to 24 of
24
with 100 items per page.
- Crouzonodermoskeletal_syndrome abstract "Crouzonodermoskeletal syndrome is a disorder characterized by the premature joining of certain bones of the skull (craniosynostosis) during development and a skin condition called acanthosis nigricans.Some of the signs and symptoms of Crouzonodermoskeletal syndrome are similar to those seen with Crouzon syndrome. They include prematurely fused skull bones, which affect the shape of the head and face; wide-set, bulging eyes due to shallow eye sockets; eyes that do not point in the same direction (strabismus); a small, beaked nose; and an underdeveloped upper jaw. People with these conditions are generally of normal intelligence.Several features distinguish Crouzonodermoskeletal syndrome from Crouzon syndrome. People with Crouzonodermoskeletal syndrome have acanthosis nigricans, a skin condition characterized by thick, dark, velvety skin in body folds and creases, including the neck and underarms. In addition, subtle changes may be seen in the bones of the spine (vertebrae). Noncancerous growths called cementomas may develop in the jaw during young adulthood.Crouzonodermoskeletal syndrome is rare; the condition is seen in about 1 per million people.".
- Crouzonodermoskeletal_syndrome wikiPageID "3442595".
- Crouzonodermoskeletal_syndrome wikiPageRevisionID "400537094".
- Crouzonodermoskeletal_syndrome hasPhotoCollection Crouzonodermoskeletal_syndrome.
- Crouzonodermoskeletal_syndrome subject Category:Genetic_disorders_with_no_OMIM.
- Crouzonodermoskeletal_syndrome type Abstraction100002137.
- Crouzonodermoskeletal_syndrome type Attribute100024264.
- Crouzonodermoskeletal_syndrome type Condition113920835.
- Crouzonodermoskeletal_syndrome type Disease114070360.
- Crouzonodermoskeletal_syndrome type GeneticDisease114151139.
- Crouzonodermoskeletal_syndrome type GeneticDisordersWithNoOMIM.
- Crouzonodermoskeletal_syndrome type IllHealth114052046.
- Crouzonodermoskeletal_syndrome type Illness114061805.
- Crouzonodermoskeletal_syndrome type PathologicalState114051917.
- Crouzonodermoskeletal_syndrome type PhysicalCondition114034177.
- Crouzonodermoskeletal_syndrome type State100024720.
- Crouzonodermoskeletal_syndrome comment "Crouzonodermoskeletal syndrome is a disorder characterized by the premature joining of certain bones of the skull (craniosynostosis) during development and a skin condition called acanthosis nigricans.Some of the signs and symptoms of Crouzonodermoskeletal syndrome are similar to those seen with Crouzon syndrome.".
- Crouzonodermoskeletal_syndrome label "Crouzonodermoskeletal syndrome".
- Crouzonodermoskeletal_syndrome sameAs m.09cnjg.
- Crouzonodermoskeletal_syndrome sameAs Q5189052.
- Crouzonodermoskeletal_syndrome sameAs Q5189052.
- Crouzonodermoskeletal_syndrome sameAs Crouzonodermoskeletal_syndrome.
- Crouzonodermoskeletal_syndrome wasDerivedFrom Crouzonodermoskeletal_syndrome?oldid=400537094.
- Crouzonodermoskeletal_syndrome isPrimaryTopicOf Crouzonodermoskeletal_syndrome.