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Síndrome de Aase-Smith; Anemia hipoplásica/síndrome del pulgar trifalángico
Es un raro trastorno que involucra anemia y ciertas deformidades esqueléticas y articulares.
La mayoría de los casos del síndrome de Aase ocurren sin una razón conocida y no se transmiten de padres a hijos (hereditario). Sin embargo, se ha demostrado que algunos casos son hereditarios.
La anemia en este síndrome es causada por el desarrollo insuficiente de la médula ósea, que es donde se forman las células sanguíneas.
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