Oculocutaneous albinism associated with axenfeld's anomaly: three case reports
SQUMJ-Sultan Qaboos University Medical Journal. 2010; 10 (1): 111-113
in English
| 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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Index:
IMEMR (Eastern Mediterranean)
Main subject:
Comorbidity
/
Consanguinity
/
Mesoderm
Type of study:
Case report
Limits:
Adolescent
/
Child
/
Humans
/
Male
Language:
English
Journal:
Sultan Qaboos Univ. Med. J.
Year:
2010
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