Download - Craneosinostosis
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CRANEOSINOSTOSIS
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Sutura frontal (metópica)
Fontanela anterior
Sutura coronal
Sutura sagital
Fontanela posterior
Sutura Lamboidea
Fontanela mastoidea
Sutura escamosaFontanela esfenoidal
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ESCAFOCEFALIA O DOLICOCEFALIA
Más frecuente.
Cierre precoz de la sutura sagital.
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BRAQUICEFALIA O TURRICEFALIA
Asocia a dismorfia facial.
Cierre precoz de la sutura coronal bilateral.
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TRIGONOCEFALIA
Asocia a holoprosencefalia.
Cierre precoz de la sutura metópica.
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PLAGIOCEFALIA
Cierre precoz de la sutura coronal unilateral.Cierre precoz de la sutura lamboidea.
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SÍNDROME DE APPERT
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Enfermedad hereditaria rara caracterizada por malformaciones encráneo, cara, manos y pies, además de diversas alteraciones funcionales.
Hereda de forma dominante y consiste en una mutación del genque codifica el receptor 2 del factor de crecimiento fibroblástico (en elbrazo largo del cromosoma 10: 10q26)
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