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- Achondroplasia_in_children abstract "Achondroplasia in children is the most common form of dwarfism; it accounts for about 70% of all cases of dwarfism. Achondroplasia falls into the category of “disproportionate dwarfism”. It is linked to a mutation in the fibroblast growth factor receptor-3. More than 250,000 people in the world are diagnosed with Achondroplasia currently. Achondroplasia diagnosis occurs somewhere between one in every 10,000 to one in every 30,000 live births. Some symptoms of Achondroplasia are short stature, long and narrow trunk, shortening of the proximal segments of limbs, large head, mid-face hypoplasia, and joint hyperextension, among other things. Achondroplasia is defined by central nervous system defects as well as the prior physical symptoms.Average height for an adult man or woman diagnosed with Achondroplasia is about 120 centimeters (47.2 inches), although technically a max of 148 centimeters (58.2 inches) is also considered Achondroplasic. Achondroplasic people typically have a long trunk and smaller upper legs and upper arms. Those diagnosed are of normal intelligence and have the ability to lead independent and productive lives.".
- Achondroplasia_in_children wikiPageExternalLink dwarfism.html.
- Achondroplasia_in_children wikiPageExternalLink restrictedgrowth.co.uk.
- Achondroplasia_in_children wikiPageID "30042152".
- Achondroplasia_in_children wikiPageRevisionID "571867965".
- Achondroplasia_in_children hasPhotoCollection Achondroplasia_in_children.
- Achondroplasia_in_children subject Category:Cell_surface_receptor_deficiencies.
- Achondroplasia_in_children subject Category:Growth_disorders.
- Achondroplasia_in_children subject Category:Pediatrics.
- Achondroplasia_in_children type Abstraction100002137.
- Achondroplasia_in_children type Attribute100024264.
- Achondroplasia_in_children type CellSurfaceReceptorDeficiencies.
- Achondroplasia_in_children type Condition113920835.
- Achondroplasia_in_children type Disorder114052403.
- Achondroplasia_in_children type GrowthDisorders.
- Achondroplasia_in_children type Lack114449405.
- Achondroplasia_in_children type Need114449126.
- Achondroplasia_in_children type PhysicalCondition114034177.
- Achondroplasia_in_children type State100024720.
- Achondroplasia_in_children comment "Achondroplasia in children is the most common form of dwarfism; it accounts for about 70% of all cases of dwarfism. Achondroplasia falls into the category of “disproportionate dwarfism”. It is linked to a mutation in the fibroblast growth factor receptor-3. More than 250,000 people in the world are diagnosed with Achondroplasia currently. Achondroplasia diagnosis occurs somewhere between one in every 10,000 to one in every 30,000 live births.".
- Achondroplasia_in_children label "Achondroplasia in children".
- Achondroplasia_in_children sameAs m.0g5b3mw.
- Achondroplasia_in_children sameAs Q4673877.
- Achondroplasia_in_children sameAs Q4673877.
- Achondroplasia_in_children sameAs Achondroplasia_in_children.
- Achondroplasia_in_children wasDerivedFrom Achondroplasia_in_children?oldid=571867965.
- Achondroplasia_in_children isPrimaryTopicOf Achondroplasia_in_children.