1.
Egyptian Journal of Hospital Medicine [The]. 2014; 55 (April): 142-145
in English
| IMEMR
| ID: emr-165985
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