A case of metageria with a review of literature
(ندگان)پدیدآور
Gharehaghaji Zare, ArmaghanGhasemi, FaranakSadri, AsalSadri, Ghazalنوع مدرک
TextCase Report
زبان مدرک
Englishچکیده
Progeroid syndromes, one of which is metageria, are characterized by signs of premature aging with multiple systemic and skin symptoms. Here we describe an 8-year-old girl with no historyof specific underlying disease in her family, no hair growth at the scalp since she was born, and taller and thinner than her peers. We noticed diffuse subcutaneous fat atrophy. The patientwas referred to Sina Hospital, Tabriz because of the appearance of pseudomilia lesions throughout the body following pulse corticosteroid therapy. Proper and timely diagnosis of progeroid syndromes is important in preventing undesirable side effects. Introducing this case is important as it prevents other patients from undergoing corticosteroid therapy due to misdiagnoses, such as alopecia areata.
کلید واژگان
acrogeriametageria
progeroid syndromes
Werner syndrome
شماره نشریه
3تاریخ نشر
2019-09-011398-06-10
ناشر
Iranian Society of Dermatologyسازمان پدید آورنده
Department of Dermatology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, IranDepartment of Dermatology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
Department of Dermatology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
Department of Radiology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran




