Biomedical subjects
K Kozlowski
Publications and source records attributed to K Kozlowski.
[Cystoid pneumatosis of the intestines in infants].
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[Radiologic pattern of the lungs in cases of mucoviscidosis in infants].
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Analysis of F wave parameters in median and ulnar nerves in healthy infants and children. Age related changes.
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Isolated unilateral clavicular hypoplasia. A case report.
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Spondylo-metaphyseal dysplasia corner fracture type (a cautionary tale).
Spondylo-metaphyseal dysplasia Sutcliffe type is a rare disease characterised by oval vertebral bodies, coxa vara and metaphyseal irregularities. It was named spondylo-metaphyseal dysplasia corner fracture type by Langer et al. as corner fractures are a constant feature later in life. We report 3 further cases of spondylo-metaphyseal dysplasia Sutcliffe type; one without coxa vara and 2 bone dysplasias with distinctive radiographic features--different from spondylo-metaphyseal dysplasia Sutcliffe type, for diagnosis. Both of the latter showed corner fractures. Corner fractures are a characteristic but not diagnostic feature of spondylo-metaphyseal dysplasia Sutcliffe type.
Dysplasia epiphysealis hemimelica: clinical features and management.
Dysplasia epiphysealis hemimelica is a rare developmental bone dysplasia characterized by an osteocartilaginous tumor arising from an epiphysis. We reviewed the clinical and radiographic findings, including magnetic resonance imaging (MRI), of nine new patients with dysplasia epiphysealis hemimelica. The lower limb was involved in all cases with the ankle (talus) and knee (distal femur) being the most common sites. MRI was helpful in defining the site and extent of the osteocartilaginous mass and provided detailed images of associated joint deformity. Often there was a clear plane of separation between the lesion and the normal epiphysis. All cases were observed initially and showed progressive increase in size of the lesion with skeletal growth. Surgical excision was performed in five cases and proved to be difficult. We recommend excision of symptomatic localized, juxtaarticular lesions but do not recommend excision of articular lesions. Postoperative degenerative joint changes occurred in two patients.
Severe pseudoachondroplasia in a mother and her son.
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