Title of article :
FREEMAN-SHELDON SYNDROME: A CASE REPORT
Author/Authors :
Salehpour ، SH. نويسنده Pediatric Endocrinologist, Department of Pediatric Endocrinology and Metabolic diseases ,Genomic Research Center, Shahid Beheshti University of Medica , , Saket ، S. نويسنده Assistant Professor of Pediatrics, Madani Children’s Hospital. Lorestan University of Medical Sciences and ,
Issue Information :
فصلنامه با شماره پیاپی - سال 2009
Abstract :
Abstract
Objective
The Freeman-Sheldon syndrome is a rare congenital myopathy and dysplasia,
in which fibrotic contractures of the facial muscles result in the characteristic
“whistling face”. Difficulties with intubation may be attributed in part to
microstomia and micrognathia. In addition to other deformities, limb myopathy
results in ulnar flexion contractures of the hand and equinovarus/valgus
deformities of the feet. Intravenous access may be difficult because of limb
deformities and thickened subcutaneous tissues. Limbs may be encased in
plaster casts or splints limiting the available sites for venepuncture. The authors
report with a review of literature the case of an infant with Freeman-Sheldon
syndrome, which his characteristics was mentioned above.
Journal title :
Iranian Journal of Child Neurology (IJCN)
Journal title :
Iranian Journal of Child Neurology (IJCN)