Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Ikkei Tamada"'
Autor:
Yoshiaki Sakamoto, MD, Hideki Amano, mEng, Naomichi Ogihara, PhD, Tomoru Miwa, MD, Ikkei Tamada, MD, Makoto Hikosaka, MD, Keisuke Imai, MD
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 12, Iss 8, p e6034 (2024)
Background:. Craniosynostosis, a common congenital anomaly, results from premature fusion of the cranial sutures. One of the forms of craniosynostosis is premature fusion of the metopic suture, referred to as trigonocephaly, but the diagnosis of meto
Externí odkaz:
https://doaj.org/article/4e495d395a284d0ab706e7cfbfcd2ec5
Publikováno v:
Journal of Plastic and Reconstructive Surgery, Vol 2, Iss 4, Pp 123-128 (2023)
Objectives: The secondary alveolar bone graft (ABG) is one of the key components in the treatment of cleft lip and palate. However, an ABG is commonly accompanied by postoperative facial edema. Although appropriate assessment of facial edema can faci
Externí odkaz:
https://doaj.org/article/a314bf83b0cd4746a21932827c96a229
Publikováno v:
Laryngoscope Investigative Otolaryngology, Vol 7, Iss 6, Pp 2126-2132 (2022)
Abstract Objectives To investigate the relationship between cleft width and otitis media (OM) and to determine whether a wide cleft palate (CP) is a risk factor of the incidence, type, amount of middle ear effusion, and prolonged morbidity in OM. Stu
Externí odkaz:
https://doaj.org/article/d57495931ec9466b8811259cbc16ad98
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 61, Iss , Pp 101626- (2020)
Bronchogenic cysts are rare congenital malformations resulting from abnormal budding of the tracheobronchial tree. We describe herein a rare case of cervical subcutaneous bronchogenic cyst found during surgery for a skin contracture in the midline of
Externí odkaz:
https://doaj.org/article/1a3e7299f89f498e9133885690f8cde0
Publikováno v:
Journal of Neurosurgery: Pediatrics. 27:69-78
OBJECTIVEThe basal encephalocele (BEC) is the rarest form of encephalocele, with an incidence of about 1/35,000 live births. The incidence of its subtype, sphenoidal BEC, is even lower at about 1/700,000 live births. The aim of this study was to prop
Publikováno v:
Child's Nervous System. 37:677-682
The present report aimed to document the clinical features of a case of Marshall-Smith syndrome (MSS), an extremely rare embryonic developmental disorder with associated craniosynostosis. We presented herein a case of a 2-year-old female patient with
Publikováno v:
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus. 26(4)
Sphenoid wing dysplasia (SWD) is a common orbital complication of neurofibromatosis type 1 (NF1). However, enophthalmos associated with SWD is extremely rare, and details of its natural history are unclear. We present the case of a 14-year-old boy wi
Publikováno v:
Journal of Craniofacial Surgery. 30:61-65
Background Growing skull fracture (GSF) is a rare, posttraumatic complication observed mainly in young infants. In GSF, the skull fracture associated with an underlying dural tear gradually expands due to herniation of the intracranial tissue into th
Autor:
Kyoji Tsuda, Tsuyoshi Kaneko, Satoshi Ihara, Kazuo Kishi, Yoshiaki Sakamoto, Makoto Hikosaka, Ikkei Tamada
Publikováno v:
The Journal of craniofacial surgery. 32(6)
Bilambdoid and sagittal synostosis (BLSS), a rare form of multisutural craniosynostosis, is sometimes known as the Mercedes-Benz syndrome due to the appearance of the fused sagittal and bilateral lambdoid sutures. Although previous studies have descr
Publikováno v:
The Journal of craniofacial surgery. 31(6)
Purpose Recently, midfacial hypoplasia for syndromic craniosynostosi has been corrected by Le Fort III distraction osteogenesis. During conventional Le Fort III osteotomy, osteotomy is performed via bicoronal incision. In contrast, the authors have d