Hallermann-streiff syndrome a case report from Egypt
Egyptian Journal of Hospital Medicine [The]. 2014; 55 (April): 142-145
em Inglês
| 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
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Índice:
IMEMR (Mediterrâneo Oriental)
Assunto principal:
Catarata
/
Microftalmia
/
Estrabismo
/
Nistagmo Congênito
/
Doenças do Recém-Nascido
Limite:
Humanos
/
Masculino
Idioma:
Inglês
Revista:
Egypt. J. Hosp. Med.
Ano de publicação:
2014
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