Hurler Syndrome
Hurler syndrome is the earliest and most pronounced form of mucopolysaccharidosis type I, a genetic disease in which the body does not properly break down certain molecules that end up accumulating in the tissues.
Common manifestations: It may become noticeable in the first years of life with distinctive facial features, joint stiffness, limited growth and involvement of several organs.
Common causes: It arises from an inherited disorder that reduces the function of an enzyme needed to process these substances.
Which specialist treats it? The pediatrician guides the child's initial evaluation and coordinates with genetics and specialists in metabolic diseases. If you notice striking signs in your child's development, the most sensible thing is to seek professional guidance early.
Specialties that treat hurler syndrome
Treatment by city
Doctors specialized in hurler syndrome
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 hurler syndrome?
Hurler syndrome is the earliest and most pronounced form of mucopolysaccharidosis type I, a genetic disease in which the body does not properly break down certain molecules that end up accumulating in the tissues.
Which doctor treats hurler syndrome?
Hurler Syndrome is usually treated by specialists in pediatrician.