Author/Authors :
Gharehaghaji Zare, Armaghan Department of Dermatology - Faculty of Medicine - Tabriz University of Medical Sciences, Tabriz, Iran , Ghasemi, Faranak Department of Dermatology - Faculty of Medicine - Tabriz University of Medical Sciences, Tabriz, Iran , Sadri, Asal Department of Dermatology - Faculty of Medicine - Tabriz University of Medical Sciences, Tabriz, Iran , Sadri, Ghazal Department of Radiology - Faculty of Medicine - Iran University of Medical Sciences, Tehran, Iran
Abstract :
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 history
of 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 patient
was 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.
Keywords :
Werner syndrome , progeroid syndromes , metageria , acrogeria