نتایج جستجو برای: unilateral coronal synostosis
تعداد نتایج: 53463 فیلتر نتایج به سال:
unilateral neglectیکی از اختلالات درک بوده و عبارتست از فراموشی یک نیمه بدن و یا نیمی از فضای اطراف در سمت مخالف ضایعه مغزی . unilateral neglectیکی از علل عمده عدم استقلال فرد در انجام فعالیتهای روزمره زندگی است . در تحقیق حاضر فرض براین بوده است که فعالیت درمانی می تواند سبب بهبود unilateral neglectو فعالیتهای روزمره زندگی دربیماران مبتلا به سکته مغزی گردد.
The purpose of this study was to determine rates of divorce in parents of children with various types of craniofacial anomalies and to analyze possible confounding factors. A 29-question survey was sent to parents of all children evaluated in the Craniofacial Centre between 1992 and 1997. Parents were questioned regarding pre- and postnatal marital stability, whether the child's facial anomaly ...
Non-syndromic bilateral humeroradial synostosis is a very rare congenital anomalies of the upper limbs. This condition often occurs in conjunction with various syndromes and is associated with a positive family history. Herein, we report a 6 year old boy with non-syndromic bilateral humeroradial synostosis, without aplasia, hypoplasia or family history. Both elbows were constant at 90 degrees f...
PURPOSE To evaluate the morphologies of congenital C2-3 synostosis in 25 patients. METHODS Radiographs of 11 males and 14 females aged 5 to 74 years with congenital C2-3 synostosis were reviewed. All cases were found incidentally on radiographs when presenting with neck/shoulder discomfort/pain. RESULTS 13 of the patients had spondylosis in 21 segments: C1-2 (n=1) and C3-4 (n=1), C4-5 (n=7)...
OBJECTIVES - To understand how surgical interventions impact the organization and internal integration of the major components of the skull, we address the functional and developmental relationships during perinatal development. METHODS - A number of methods for quantifying modularity and integration of morphological data are available. Here, measures derived from three-dimensional computed tom...
Apert syndrome is an autosomal dominantly inherited disorder caused by missense mutations in fibroblast growth factor receptor 2 (FGFR2). Surgical procedures are frequently required to reduce morphological and functional defects in patients with Apert syndrome; therefore, the development of noninvasive procedures to treat Apert syndrome is critical. Here we aimed to clarify the etiological mech...
The aim of this study is to determine the different therapeutic options described for the treatment of radioulnar synostosis, and report our experience with posterior interosseous antegrade flow pedicled flap with technical amendments. Two patients, who were treated with the designed flap, and with more than one year of follow-up, were reviewed. The technical innovations, end result and complic...
We report on a patient with humeroradioulnar synostosis and lambdoid synostosis. The case differs from three previously described cases in minor details, but the upper limb abnormalities are strikingly similar.
Synostosis or osseous union of any 2 adjacent bones can involve any part of the body. Synostosis between radius and ulna can take two forms, congenital and post Synostosis is a very rare congenital anomaly and most cases a post-traumatic, bilateral in 60% and more common in males. It is often part of syndromes such as Crouzon, Apert's and Poland's,4p Bixler syndrome, Genito multiple osteochondr...
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