Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Salim N Mancho"'
Autor:
Spencer R. Anderson, Salim N Mancho
Publikováno v:
Journal of Craniofacial Surgery. 32:e587-e589
Noonan syndrome is a rare, autosomal dominant disorder encompassing multiple congenital defects, as well as association with solid tumor and lesion development. The authors present a 26-year-old female with known Noonan syndrome and ongoing complaint
Autor:
Salim N Mancho, Kaitlynne Y. Pak, Kelly E. Spiller, Spencer R. Anderson, Lucas M. Harrison, Steven P. Schmidt
Publikováno v:
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association. 59(4)
Complete congenital arhinia is a rare defect of embryogenesis leading to the absence of the external nose and airway. We report our novel multistaged reconstructive approach and literature review. Nasal methyl methacrylate prosthesis was created from
Publikováno v:
Neurosurgical focus: Video. 4(2)
The authors describe the use of the Gigli saw for craniectomy in minimal access surgery to address sagittal craniosynostosis. This modification allows for supine positioning and avoidance of potential brain compression with endoscopic instruments, an
Autor:
Brandon R. Horne, Sunishka M. Wimalawansa, Salim N Mancho, Spencer R. Anderson, Garyn T Metoyer
Publikováno v:
JBJS Case Connector. 10:e0496-e0496
Case We discuss our reconstructive approach to avoid an above-knee amputation in a 33-year-old man presenting after lower extremity crush injury. We used a vascularized tibial bone flap and a foot fillet flap to restore length and joint functionality
Autor:
Whittney A, Warren, Nicole C, Droz, Sunishka M, Wimalawansa, Salim N, Mancho, Jack M, Bernstein
Publikováno v:
Skinmed. 14(1)
Autor:
Elizabeth Rommer, Joseph N. Carey, Mark M. Urata, Cameron S. Francis, Salim N Mancho, Jeffrey A. Hammoudeh
Publikováno v:
Journal of Craniofacial Surgery. 23:S58-S61
Le Fort III and monobloc distraction osteogenesis serve as the primary surgical treatment for children with severe midface hypoplasia. The orbital retrusion and class III malocclusion of patients with midface hypoplasia is best addressed with bodily