The mucopolisacaridosis (MPS) is a group of hereditary metabolic diseases caused by the onset or malignancy of enzymes, within which Morquio’s syndrome is located which consists of a hereditary metabolic disorder.
Daniela Osorio Rivera
Agencia Latina de Noticias Medicina y Salud Pública
In agreement with the medical review and Public Health Review, Dr. Heriberto Román, Coordinator of the San Jorge Children’s Clinical Research Center, spoke about morbidity syndrome and its consequences.
In the majority of MPS no neonatal sclerosis is observed, these are taken into account when the nines are ten years old and the diagnosis is confirmed by means of a panel of mucopolisacaridosis by blood.
” Inside of the first signs that are observed by the general his anomalies on the road, abnormal position of the roads, deformation of the toxic road or the most slow crime. The physical characteristics that can be included include: disproportionate stature with shortened trunk, short cortex, braces and broken legs, contractures in the flexion of the frame and facial grooming. ”, Explained the Dr.
Morquio’s syndrome is a recessive autosomal process that requires that there be a variety of ways in which speed, transmission or transmission can be transmitted to parents.
Historically the majority of patients mueren prematurely. The risks are clearly related to the severity of the spinal dysfunction due to cervical compression, restrictive pulmonary disease and cardiac disease as well as the effective treatment of the diseases.
” Many women who suffer from this disorder live in their normal way without embarrassment Many of you can read some respiratory compromises and are obliged to recover for a period. ”, Añadió el Dr.
The baby’s training at the time of birth is normal and his birth rate continues to change during the first and second year of life, after the third year he has experienced more. The linear development takes place between 7 and 12 years of age, it is very important to be able to determine its treatment of enzymatic replacement and perform certain surgical interventions.
” The maximum stature of a person who has this syndrome oscillates between 80 and 140 cm, without embarrassment, has a stature that means that the patient has certain needs that affect his diary live for the rest of his life. ”, Mencionó el Dr.
Consequences
The intellectual capacity differs from the other types of mucopolysaccharidosis as normal, although there are other complications. the articles.
In addition, those affected frequently have corneal opacity, a sign that there is usually no condition and that causes some problems. Experience suggests that surgical intervention is an option in more severe cases, although recurrence may exist. It’s very rare to see other ocular complications such as glaucoma or cataracts ”, explained Dr.
The loss of the audition by the general public to the children’s mediators, an affection that is also presented as a progressive progressive loss in moderation. In those affected with this syndrome, it is a dysfunction of the medium. An audiological evaluation should be carried out at least once a year, at the beginning of the diagnosis and continuously throughout the patient’s life.
On the other hand the esmalte dental is uniformly abnormal, this condition affects both the teeth of leches as the permanent ones, there is a mayor probability of dental fractures, dental desgaste and caries.
The respiratory problems of restrictive and obstructive characteristics can be surpassed in patients with morbidity syndrome, it is fundamental to carry out medical visits to the neurologist and the specialist in somnology with the help to define the appropriate treatments according to the need.
With adequate treatment, many people affected by morning sickness have grown up during adulthood, but there are also cases where patients undergo 50 or 60 years of life.