Mucopolysaccharidosis Type I-S
Mucopolysaccharidosis type I S is a rare disease of genetic origin in which the body does not properly process certain complex molecules, which accumulate in the tissues. It is part of a broader group of metabolic disorders.
How does it manifest? It is usually associated with joint involvement, stiffness, changes in facial features, and vision impairment, with an evolution that varies among people.
Why is it important to recognize it? Since it is a hereditary condition, identifying it in time allows for organizing comprehensive follow-up and guiding the family.
Who treats it? The pediatrician accompanies the patient from early stages and coordinates the evaluation with other professionals according to the affected organs. If there is a family history or suggestive signs, it is advisable to seek a specialized evaluation.
Specialties that treat mucopolysaccharidosis type i-s
Treatment by city
Doctors specialized in mucopolysaccharidosis type i-s
Dr. Edgar Bustos Córdova
Dr. Alberto Fregoso Ojeda
Dr. Rodolfo Rivas Ruiz
Dr. Sergio Miguel Gomez Dorantes
Dr. Mercado Filomena Vizcaino
Dr. Olga Eugenia Martínez Garza
Dr. Jose Luis Balanzar Serna
Dr. Alfonso Corona Tellez
Dr. Rodriguez Francisco Herrera
Dr. Román Pineda Abarca
Dr. Escandon Hector Calles
Dr. Roberto Moreno Paez
Dr. Francisco Alvarado Alemán
Dr. Jesús Isidro Pinzón Sánchez
Dr. Elizabeth Solano Pareja
Dr. Victor Tapia Alfaro
Dr. Julio Fraire Calleros
Dr. Gabriela Juárez Domínguez
Dr. Maria Eugenia Chang Gonzalez
Dr. Edgar Sanchez-Uribe
Frequently asked questions
What is mucopolysaccharidosis type i-s?
Mucopolysaccharidosis type I S is a rare disease of genetic origin in which the body does not properly process certain complex molecules, which accumulate in the tissues. It is part of a broader group of metabolic disorders.
Which doctor treats mucopolysaccharidosis type i-s?
Mucopolysaccharidosis Type I-S is usually treated by specialists in pediatrician.