MUCOPOLISACARIDOSIS TYPE I: HURLER SYNDROME ABOUT A CASE

Authors

  • Dra. Raquel Moreno Lora, Neuróloga Infantil, “Instituto Psicopedagógico: San Juan de Dios”
  • Dra. Valeria Aillón López, Médico Adscrito, Servicio de Neurología. “Instituto Psicopedagógico: San Juan de Dios”

Keywords:

Mucopolysaccharidosis, Hurler Syndrome, Diagnosis, treatment, prognosis

Abstract

This article presents the case of a child of 10 years old, attended a neurology derived from the TSI (School Integration Workshop) of Monteagudo, which attended physiotherapy. The reference was made to opt for some guidelines for better unwrapped physiotherapist’s growth and development in their environment was so incidentally occurred with this particular pathology. The diagnosis is based almost done on family history, clinical and CT of skull simple. While I request all necessary tests, especially the genetic study, which unfortunately got support by the aforementioned institution could not cover all the analytical and relatives do not have sufficient financial resources. Hence, we motivated the literature review Mucopolisacariodosis Type I Hurler perspective of diagnosis, treatment and hopefully contribute some concerns that somehow.

As a condition to the international literature does not report many cases.

Published

2019-10-23

How to Cite

Moreno Lora, D. R., & Aillón López, D. V. (2019). MUCOPOLISACARIDOSIS TYPE I: HURLER SYNDROME ABOUT A CASE. Revista Del Instituto Médico Sucre, 78(140/141), 43–46. Retrieved from https://revistas.usfx.bo/index.php/ims/article/view/241