Oculocutaneous albinism associated with axenfeld's anomaly: three case reports
SQUMJ-Sultan Qaboos University Medical Journal. 2010; 10 (1): 111-113
en Inglés
| IMEMR
| ID: emr-98051
ABSTRACT
Oculocutaneous albinism and anterior mesodermal dysgenesis are well-known heritable conditions, but their occurrence in association has only been rarely reported. We present cases of three siblings of a family with identical presentation suggesting that this association may be more than just a coincidence. This association is worth noting, as this could be one of the causes of ocular morbidity and poor vision in oculocutaneous albinism
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Índice:
IMEMR (Mediterraneo Oriental)
Asunto principal:
Comorbilidad
/
Consanguinidad
/
Mesodermo
Tipo de estudio:
Informe de Casos
Límite:
Adolescente
/
Niño
/
Humanos
/
Masculino
Idioma:
Inglés
Revista:
Sultan Qaboos Univ. Med. J.
Año:
2010
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