Ophthalmology department, Faculty of Medicine (For Girls), Al Azhar University
10.12816/0004499
Abstract
Abstract
Hallermann-Streiff syndrome (HSS) is a rare genetic disorder that is primarily characterized by distinctive malformations of the skull and facial (craniofacial) region; sparse hair (hypotrichosis); eye abnormalities; dental defects; degenerative skin changes (atrophy), particularly in the scalp and nasal regions; and proportionate short stature. Here we describe a case with HSS.
Atwa, F. A., Farag, M. M., Mansour, M. N., & Albadry, A. F. (2014). Hallermann-Streiff syndrome A case report from Egypt. The Egyptian Journal of Hospital Medicine, 55(1), 142-145. doi: 10.12816/0004499
MLA
Fatma A. Atwa; Mona M.A. Farag; Mona N. Mansour; Abeer F. Albadry. "Hallermann-Streiff syndrome A case report from Egypt", The Egyptian Journal of Hospital Medicine, 55, 1, 2014, 142-145. doi: 10.12816/0004499
HARVARD
Atwa, F. A., Farag, M. M., Mansour, M. N., Albadry, A. F. (2014). 'Hallermann-Streiff syndrome A case report from Egypt', The Egyptian Journal of Hospital Medicine, 55(1), pp. 142-145. doi: 10.12816/0004499
VANCOUVER
Atwa, F. A., Farag, M. M., Mansour, M. N., Albadry, A. F. Hallermann-Streiff syndrome A case report from Egypt. The Egyptian Journal of Hospital Medicine, 2014; 55(1): 142-145. doi: 10.12816/0004499
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