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Klin Padiatr ; 221(5): 308-9, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19707994

ABSTRACT

This article is about a 9-year-old boy with known homozygous sickle cell disease who developed unilateral exophthalmia and eyelid swelling during a sickle cell crisis. The symptoms were due to a vaso-occlusive event in the orbital bones,known as orbital compression syndrome, which is a rare complication of sickle cell disease.


Subject(s)
Anemia, Sickle Cell/diagnosis , Arterial Occlusive Diseases/diagnosis , Exophthalmos/diagnosis , Orbital Diseases/diagnosis , Anemia, Sickle Cell/therapy , Anti-Bacterial Agents/therapeutic use , Arterial Occlusive Diseases/therapy , Blood Transfusion , Child , Diagnosis, Differential , Drug Therapy, Combination , Edema/diagnosis , Exophthalmos/therapy , Femur Head Necrosis/diagnosis , Femur Head Necrosis/therapy , Humans , Magnetic Resonance Imaging , Male , Orbit/blood supply , Orbit/pathology , Orbital Diseases/therapy
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