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Achondroplasia

More information in Books or onNLM PubMed
Definition: An autosomal dominant disorder that is the most frequent form of short-limb dwarfism. Affected individuals exhibit short stature caused by rhizomelic shortening of the limbs, characteristic facies with frontal bossing and mid-face hypoplasia, exaggerated lumbar lordosis, limitation of elbow extension, GENU VARUM, and trident hand. (Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim, MIM#100800, April 20, 2001)     
See Also Receptor, Fibroblast Growth Factor, Type 3
Examples Thanatophoric Dysplasia
Other names Severe Achondroplasia with Developmental Delay and; SADDAN Dysplasias; Dysplasias, SADDAN; Dysplasia, SADDAN; Achondroplasias; SADDAN Dysplasia
 
SubstanceCAS Registry & nameCategoriesSource
Dyssegmental dysplasia, Rolland-Desbuquois type  0   *Achondroplasia *Cleft Palate *Campomelic Dysplasia.
Baby rattle pelvic dysplasia  0   *Achondroplasia Bone and Bones Fetus/abnormalities.
Achondroplasia and Swiss type agammaglobulinemia  0   *Achondroplasia *Agammaglobulinemia.
Achondrogenesis, type 4  0   *Achondroplasia.
Achondrogenesis, type 3  0   *Achondroplasia.
Achondrogenesis type 2  0   *Achondroplasia.
Achondrogenesis type 1B  0   *Achondroplasia.
Achondrogenesis type 1A  0   *Achondroplasia.
Pseudoachondroplastic dysplasia 2  0   *Achondroplasia.
Pseudoachondroplasia  0   *Achondroplasia.
Achondroplastic dwarfism  0   *Achondroplasia.

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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