Neuropatía sensorial y autonómica hereditaria: un caso clínico

Contenido principal del artículo

MD Lilem Valerio-Gil
MD Laura Segura-Agüero

Keywords

Neuropatías Hereditarias Sensoriales y Autónomas, Dolor Congénito

Resumen

Las neuropatías sensoriales y autonómicas hereditarias, como el tipo IV, presentan desafíos clínicos al afectar la percepción del dolor y la temperatura, junto con anhidrosis. En este contexto, se informa sobre un joven de 17 años con este diagnóstico desde los 8 años. Su historial médico incluye fracturas, artritis y osteomielitis por traumas leves, resultando en ingresos hospitalarios extensos con múltiples intervenciones quirúrgicas y episodios sépticos. Aunque exhibe independencia parcial en las actividades diarias, no hay tratamiento específico, y el manejo se centra en el apoyo, la identificación temprana de problemas y la prevención de complicaciones. Destacamos la importancia del diagnóstico precoz para mejorar la gestión y el pronóstico de estos pacientes.

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Citas

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