نتایج جستجو برای: occipital dysplasia
تعداد نتایج: 41300 فیلتر نتایج به سال:
BACKGROUND Ectodermal dysplasia (ED) is a hereditary syndrome which affects the ectodermal layer and thus appendages originating from this layer like hair, teeth, and sweet glands. The hairs of the scalp and eyebrows are sparse and broken and sometimes absent in ED patients. We reported a case of ED who underwent successful hair transplantation for her eyebrows. CASE REPORT A 17-year-old fema...
BACKGROUND Sex chromosomal aneuploidies in males are rare diseases with an overwhelming involvement of endocrinological and auxological issues; less frequently, other anomalies are observed. Neuroradiological issues are often not taken into account in single patients, and neuroradiological examinations are rarely performed. CASE PRESENTATION Here, we report a boy with 48,XXXY/49,XXXXY mosaici...
Blindness attributed to vitamin A deficiency afflicted 47 out of 197, and 15 out of 29 new-born dairy calves on 2 farms. Other clinical signs included doming of the forehead, thickening of the carpal joints, incoordination and weakness. Gross lesions in 8 of the calves examined consisted in hydrocephalus and thickened occipital and sphenoid bones. In 4 of these calves the optic nerves were cons...
A 14-year-old was girl admitted to our hospital with a subcutaneous mass of the occipital head. The mass had grown for 6 years, after she had sustained a head injury at the age of 6, and was located directly under a previous wound. Skull X-ray Photograph (xp), computed tomography (CT), and magnetic resonance imaging (MRI) showed a bony defect and cystic changes in the skull corresponding to a s...
Developmental dysplasia of the hip (DDH) or congenital hip dysplasia (CDH) is the most prevalent developmental childhood hip disorder. It includes a wide spectrum of hip abnormalities ranging from dysplasia to subluxation and complete dislocation of the hip joint. The natural history of neglected DDH in adults is highly variable. The mean age of onset of symptoms is 34.5 years for dysplastic DD...
This is a brief report of a stillborn infant with a spectrum of distinctive congenital malformations. Although the family history and pregnancy gave no clue as to the aetiology of the malformations, we believe a description is warranted because the findings are so dramatic that, if further cases occur (or have occurred), they should be readily recognised and thus perhaps a syndrome could be del...
Background & objective: Changes in submucosal vascularization and inflammation, determined by immunohistochemistry staining, were shown to be correlated with the development of dysplasia and invasiveness of epithelial cells in premalignant and malignant lesions. This study evaluated changes in sections routinely stained with Hematoxylin and Eosin (H&E;) in orde...
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