ALLMedicine™ Atelosteogenesis Type 2 Center
Research & Reviews 3 results
https://www.ncbi.nlm.nih.gov/books/n/gene/ao2/
Sep 23rd, 2020 - Clinical features of atelosteogenesis type 2 (AO2) include rhizomelic limb shortening with normal-sized skull, hitchhiker thumbs, small chest, protuberant abdomen, cleft palate, and distinctive facial features (midface retrusion, depressed nasal b...
https://rarediseases.info.nih.gov/diseases/8329/atelosteogenesis-type-2
Dec 16th, 2013 - Atelosteogenesis type 2 is a genetic disorder that affects cartilage and bone development. Infants born with this condition have very short arms and legs, a narrow chest, and a prominent, rounded abdomen. The signs and symptoms of atelosteogenesis...
https://doi.org/10.1111/j.1399-0004.2010.01595.x
Clinical Genetics; Barbosa M, Sousa AB et. al.
Dec 15th, 2010 - SLC26A2-related dysplasias encompass a spectrum of diseases: from lethal achondrogenesis type 1B (ACG1B; MIM #600972) and atelosteogenesis type 2 (AO2; MIM #256050) to classical diastrophic dysplasia (cDTD; MIM #222600) and recessive multiple epip...
Clinicaltrials.gov 3 results
https://www.ncbi.nlm.nih.gov/books/n/gene/ao2/
Sep 23rd, 2020 - Clinical features of atelosteogenesis type 2 (AO2) include rhizomelic limb shortening with normal-sized skull, hitchhiker thumbs, small chest, protuberant abdomen, cleft palate, and distinctive facial features (midface retrusion, depressed nasal b...
https://rarediseases.info.nih.gov/diseases/8329/atelosteogenesis-type-2
Dec 16th, 2013 - Atelosteogenesis type 2 is a genetic disorder that affects cartilage and bone development. Infants born with this condition have very short arms and legs, a narrow chest, and a prominent, rounded abdomen. The signs and symptoms of atelosteogenesis...
https://doi.org/10.1111/j.1399-0004.2010.01595.x
Clinical Genetics; Barbosa M, Sousa AB et. al.
Dec 15th, 2010 - SLC26A2-related dysplasias encompass a spectrum of diseases: from lethal achondrogenesis type 1B (ACG1B; MIM #600972) and atelosteogenesis type 2 (AO2; MIM #256050) to classical diastrophic dysplasia (cDTD; MIM #222600) and recessive multiple epip...
