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Sindrome de Crouzon: Verdades y mentiras

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Desafía tus conocimientos sobre el Síndrome de Crouzon

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Costa Rica

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Sindrome de Crouzon: Verdades y mentiras
 

Sindrome de Crouzon: Verdades y mentirasOnline version

Desafía tus conocimientos sobre el Síndrome de Crouzon

by Yosebeth Jara
1

En muchos casos, las personas con síndrome de Crouzon mantienen una inteligencia dentro de la media de su edad de desarrollo.

2

Las mutaciones en los genes FGFR2, o en FGFR3, pueden estar implicadas en este síndrome.

3

Se suele presentar con signos visibles al nacimiento y son evidentes desde el parto.

4

Las malformaciones orbitarias pueden provocar exoftalmos, es decir, ojos protuberantes.

5

El paladar hendido y las deformidades faciales son raros y no suelen aparecer.

6

La mutación asociada se encuentra en el gen FGFR2 en el cromosoma 12.

7

El síndrome no afecta la respiración ni la alimentación de los pacientes.

8

El síndrome de Crouzon es un trastorno genético caracterizado por craneosinostosis prematura.

9

La craneoplastia u otras cirugías pueden ayudar a corregir la deformidad y aliviar la presión intracraneal.

10

El síndrome de Crouzon tiene cura definitiva y no requiere seguimiento médico.

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