Results 161 to 170 of about 7,211 (209)
Adult post-traumatic radioulnar synostosis [PDF]
Orthopaedics and Traumatology: Surgery and Research, 2012 SummaryPost-traumatic radioulnar synostosis is a rare complication of forearm fracture. Resulting in loss of forearm axial rotation, it is functionally very disabling. The surgical indication, timing of operation, surgical technique, interest and type of
F Khiami, Jean-Noël Goubier
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The Journal of Pediatrics, 2019
Unicoronal synostosis presents with a characteristic head shape including a palpable ridge over the fused suture, ipsilateral flattening of the frontal bone and bulging of the temporal bone, contralateral bulging of the frontal bone, deviation of the nasal radix to the ipsilateral side, and anterior displacement of the ipsilateral ear.
Frank, Weng +2 more
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Unicoronal synostosis presents with a characteristic head shape including a palpable ridge over the fused suture, ipsilateral flattening of the frontal bone and bulging of the temporal bone, contralateral bulging of the frontal bone, deviation of the nasal radix to the ipsilateral side, and anterior displacement of the ipsilateral ear.
Frank, Weng +2 more
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Congenital Radioulnar Synostosis
Journal of the American Academy of Orthopaedic Surgeons, 2021Congenital radioulnar synostosis is a rare condition resulting in fusion of the proximal portions of the radius and ulna. Patients commonly present in early childhood with functional deficits because of limited forearm rotation and fixed positioning of the forearm. Compensatory motion and hypermobility are frequently observed at the wrist and shoulder,
Paul T. Rutkowski, Julie Balch Samora
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Length of synostosis and segmented intracranial volume correlate with age in patients with non-syndromic sagittal synostosis [PDF]
Child's Nervous System, 2017 The aim of this study is to compare the length of synostosis and segmented intracranial volume (SIV) with age in children with non-syndromic sagittal synostosis.
Arja Heliövaara +2 more
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Hand Clinics, 1994
Radioulnar synostosis is a rare condition that exists in two forms: congenital and post-traumatic. Although both may involve either a bony or a fibrous union between the radius and ulna, they differ considerably in their etiologies, treatment, and prognosis. This article explores both of these conditions.
K, Sachar, E, Akelman, M G, Ehrlich
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Radioulnar synostosis is a rare condition that exists in two forms: congenital and post-traumatic. Although both may involve either a bony or a fibrous union between the radius and ulna, they differ considerably in their etiologies, treatment, and prognosis. This article explores both of these conditions.
K, Sachar, E, Akelman, M G, Ehrlich
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Clinics in Plastic Surgery, 1994
Sagittal synostosis comprises a spectrum of deformities caused by premature fusion of the sagittal suture. The treatment of sagittal synostosis is dependent on the age of the patient and the characteristics of the presenting deformity. Immediate correction of the scaphocephalic deformity is the goal of operative treatment.
R V, Ocampo, J A, Persing
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Sagittal synostosis comprises a spectrum of deformities caused by premature fusion of the sagittal suture. The treatment of sagittal synostosis is dependent on the age of the patient and the characteristics of the presenting deformity. Immediate correction of the scaphocephalic deformity is the goal of operative treatment.
R V, Ocampo, J A, Persing
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Clinics in Plastic Surgery, 1994
Recent increases in presentation of occipital deformities have presented the craniofacial team with new challenges in diagnosis and treatment. As presented in this article, they appear to have a functional abnormality of the suture that results in a localized growth deformity.
C A, Vander Kolk, B S, Carson
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Recent increases in presentation of occipital deformities have presented the craniofacial team with new challenges in diagnosis and treatment. As presented in this article, they appear to have a functional abnormality of the suture that results in a localized growth deformity.
C A, Vander Kolk, B S, Carson
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Humeroradial synostosis and the multiple synostosis syndrome: case report
Journal of Pediatric Orthopaedics, Part B, 2003Humeroradial synostosis may occur sporadically or as an extremely rare inheritable disorder. The current classification divides cases into class I (fixed in extension with ulnar ray hypoplasia) or class II (fixed in flexion without hypoplasia). Familial cases of class II synostosis segregate into autosomal recessive and autosomal dominant groups ...
James D, McIntyre +2 more
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European Journal of Pediatrics, 1980
A 2-year-old deeply mentally handicapped girl is reported with a multiple synostosis syndrome, as delineated by Maroteaux et al. (1972). Besides the multiple synostoses the peculiar facial dysmorphism and the hearing deficit allow, the clinical diagnosis of this apparently rare syndrome.
J C, Pedersen +4 more
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A 2-year-old deeply mentally handicapped girl is reported with a multiple synostosis syndrome, as delineated by Maroteaux et al. (1972). Besides the multiple synostoses the peculiar facial dysmorphism and the hearing deficit allow, the clinical diagnosis of this apparently rare syndrome.
J C, Pedersen +4 more
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Clinical Genetics, 1978
A sporadic case of humero‐radial synostosis is reported in an infant in whom no other congenital malformations were found. The mode of inheritance of humero‐radial synostosis in our case is not clear, but it might be autosomal recessive.
R B, Surana, S M, Sinkford
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A sporadic case of humero‐radial synostosis is reported in an infant in whom no other congenital malformations were found. The mode of inheritance of humero‐radial synostosis in our case is not clear, but it might be autosomal recessive.
R B, Surana, S M, Sinkford
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