Morchuvio syndrome infected by a patient who carried out an unpublished operation in Italy

San Kamilo Forlanini Hospital in Rome was recently produced For the first time in history worldwide a Morguvio Syndrome In particular, this process was already implemented in the implementation of another new cortex bioprostasis.

One of the most important aspects of the procedure is that the 53 -year -old patient suffers from the syndrome of Morguvio, which is a hereditary pathology Prevents holding the necessary enzymes To break the long chains of sugar molecules, they can accumulate, cause many health problems, such as the abnormal growth of the bones or the malfunction of certain important organs.

What, what are your symptoms

The Chile Magazine of Pediatrician belongs to Morguvio’s syndrome, belonging to MucopoliSagidosis, which is in a group Low -damage diseases At the lesomal level, the deficiency of enzymes participating in the metabolism of glucosaminglukunos (GAG) is characterized by the lack of the leasomal level. As a result, these molecules accumulate in space between cells and cause many health problems that affect different organs and systems.

Morguvio’s syndrome Category IV mucopolisagarides. There are two sub -types: A and B, depending on what the metabolic molecules are affected.

In both cases, changes begin to be observed Between the first and the third year of life. The lower height, the short stem, Chest hinge . There is joint hyperlaxity in the hip level, the lower ends, the genu valco and the flat foot; And the spinal changes may shorten the marrow and create progressive weakness and stroke. Psychomotor and intellectual development is normal.

How is Morguvio syndrome

Patients with Morguvio syndrome Enjoy a variety of problemsIt can vary according to the severity of the disease and according to the age of the patient.

There is no treatment at present for the disease, so the attitude is based on Altermatotherapy And in the practice of surgical interventions to solve complications.

Notes

George Louis Suarez-Grero, Point Pedro Jose Ivan Gomez Hikuwera, Juan Sebastian Ariyas Flarez, Gustavo Adolpo Contrasrez-Carcia. MagaropoliSagidosis: Medical, Diagnosis and Management Properties. Chile Chile Pediatric Magazine (2015). DOI: 10.1016/j.rchipe.2015.10.004

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