Hallermann-Streiff syndrome A case report from Egypt | ||||
| The Egyptian Journal of Hospital Medicine | ||||
| Article 3, Volume 55, Issue 1, April 2014, Page 142-145 PDF (424.11 K) | ||||
| Document Type: Original Article | ||||
| DOI: 10.12816/0004499 | ||||
 View on SCiNiTO | ||||
| Authors | ||||
| Fatma A. Atwa; Mona M.A. Farag; Mona N. Mansour; Abeer F. Albadry | ||||
| Ophthalmology department, Faculty of Medicine (For Girls), Al Azhar University | ||||
| 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. | ||||
| Keywords | ||||
| Hallermann-Streiff syndrome; congenital cataract; Microphthalmos | ||||
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