A family affected with Blepharophimosis syndrome
<p>Blepharophimosis syndrome is a genetic disease characterized by a shortening of the palpebral fissure or blepharophimosis, associated to ptosis and epicanthus inversus in most cases. The disease is transmitted in an autosomal dominant form with two well-identified clinical types. This is a...
| Main Authors: | , |
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| Format: | Article |
| Language: | Spanish |
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Universidad de Ciencias Médicas de Las Tunas
2016-02-01
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| Series: | Revista Electrónica Dr. Zoilo E. Marinello Vidaurreta |
| Subjects: | |
| Online Access: | http://revzoilomarinello.sld.cu/index.php/zmv/article/view/623 |