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1.
Indian J Pediatr ; 2000 Jun; 67(6): 471-2
Artículo en Inglés | IMSEAR | ID: sea-82065
2.
Indian J Pediatr ; 1999 May-Jun; 66(3): 455-60
Artículo en Inglés | IMSEAR | ID: sea-78967

RESUMEN

Progressive pseudorheumatoid arthropathy of childhood (PPAC) described by Spranger et al is a rare autosomal recessive disorder. An 11 year-old girl was diagnosed as having PPAC at Ege University, Faculty of Medicine, Department of Paediatrics. Her complaints of painful joints, difficulty in walking and joint contractures began at the age of 3 years and she was treated for juvenile rheumatoid arthritis for 8 years. Her symptoms did not respond to nonsteroid anti-inflammatory treatment. During her last hospitalisation period, she was reinvestigated. Radiological examination showed spondyloepiphyseal dysplasia, severe acetabular irregularity and osteoporosis. All the laboratory test results for rheumatoid arthritis were negative. The clinical and radiological findings of the patient are illustrated.


Asunto(s)
Acetábulo/patología , Antiinflamatorios no Esteroideos/uso terapéutico , Artritis Juvenil/diagnóstico , Niño , Contractura/diagnóstico , Diagnóstico Diferencial , Femenino , Humanos , Lordosis/diagnóstico , Vértebras Lumbares/patología , Osteocondrodisplasias/diagnóstico , Osteoporosis/diagnóstico
3.
Indian J Pediatr ; 1997 Jan-Feb; 64(1): 113-6
Artículo en Inglés | IMSEAR | ID: sea-80747

RESUMEN

Severely involved female child with Multiple Pterygium Syndrome (Escobar) is described. She had the typical findings of the syndrome such as multiple pterygiums, characteristic facial appearance, genital anomalies. She also had bilateral optic atrophy. This is the first case described so far with optic atrophy in Multiple Pterygium Syndrome (Escobar).


Asunto(s)
Anomalías Múltiples/diagnóstico , Brazo/anomalías , Atrofia , Niño , Consanguinidad , Cara/anomalías , Femenino , Deformidades Congénitas del Pie/diagnóstico , Genitales Femeninos/anomalías , Humanos , Nervio Óptico/patología , Pterigion/diagnóstico , Columna Vertebral/anomalías , Síndrome
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