eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | acrocephalosyndactyly |
| Comorbidity | C0010278|craniosynostosis |
| Sentences | 5 |
| PubMedID- 25191197 | Anesthetic management of craniosynostosis repair in patient with apert syndrome. |
| PubMedID- 22337402 | craniosynostosis in apert syndrome is routinely treated by wide frontal and bilateral supraorbital reshaping and posterior cranial decompression. |
| PubMedID- 25003957 | Thus, based on our current data, we suggest that increased fgf10 and fgfr2iiib expression may induce the onset of craniosynostosis in patients with apert syndrome and that the appropriate delivery of purified sfgfr2iiics252w could be effective for treating this disorder. |
| PubMedID- 21354088 | A full-term female baby was diagnosed as having apert syndrome with craniosynostosis, hypertelorism, syndactyly, polydactyly, and cleft plate. |
| PubMedID- 26543480 | Erratum: anesthetic management of craniosynostosis repair in patient with apert syndrome: erratum. |
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