Congenital pseudoarthrosis of the clavicle with bifurcation
نویسندگان
چکیده
منابع مشابه
Congenital Pseudoarthrosis of the Clavicle
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متن کامل[Congenital pseudoarthrosis of the clavicle in a boy with Prader-Willi's syndrome].
The authors present the case of a boy with congenital pseudoarthrosis of the right clavicle who met all clinical and auxologic criteria of Prader-Willi's syndrome. Poor cooperation due to mental retardation was the reason for the primary conservative treatment. During this, deformity of the middle clavicle progressed, but without development of subjective complaints and functional deficit. At h...
متن کاملCongenital pseudoarthrosis of clavicula.
Right clavicula fracture was found in a male patient who was brought to our outpatient clinic at the age of 7 days with a complaint of swelling on the right clavicula. The patient had no history of difficult delivery or resuscitation. He was born at term by spontaneous vaginal delivery with a birth weight of 3 340 g from the first pregnancy of his mother and there was no consanguinity between t...
متن کاملCongenital Pseudarthrosis of the Clavicle
Congenital pseudarthrosis of the clavicle is a rare condition and after being reported for the first time in 1910, only about 200 cases have been reported in literature in last hundred years. The condition is predominantly right sided and etiology is still unclear. Imaging plays a vital role in diagnosis and subsequent management. Surgical management comprises of excision of pseudarthrosis with...
متن کامل[Congenital pseudarthrosis of the clavicle].
A case of congenital pseudarthrosis of the clavicle is presented. Congenital pseudarthrosis of the clavicle is a rare entity that has poorly been documented in the pediatric literature. The etiology and pathogenesis still remain obscure. The clinical and radiological appearances are characteristic. Differential diagnosis lies between postpartum fracture, posttraumatic pseudarthrosis, cleidocran...
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ژورنال
عنوان ژورنال: Indian Journal of Orthopaedics
سال: 2014
ISSN: 0019-5413
DOI: 10.4103/0019-5413.136314