Galactosamine-6-Sulfatase Deficiency
Galactosamine-6-sulfatase deficiency is a rare inherited disorder, known as Morquio syndrome type A, in which the lack of an enzyme prevents the processing of certain substances that build up in the body's tissues.
What it involves: This buildup affects mainly the development of the bones and joints, and can have repercussions on growth, mobility and other organs.
Origin: It has a genetic cause and is passed from parents to children, so its signs are usually noticed during childhood.
Which specialist treats it? The pediatrician performs the initial assessment and relies on geneticists and other specialists for developmental follow-up. If changes in a child's bone growth are observed, it is advisable to raise them with a professional for evaluation.
Specialties that treat galactosamine-6-sulfatase deficiency
Treatment by city
Doctors specialized in galactosamine-6-sulfatase deficiency
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 galactosamine-6-sulfatase deficiency?
Galactosamine-6-sulfatase deficiency is a rare inherited disorder, known as Morquio syndrome type A, in which the lack of an enzyme prevents the processing of certain substances that build up in the body's tissues.
Which doctor treats galactosamine-6-sulfatase deficiency?
Galactosamine-6-Sulfatase Deficiency is usually treated by specialists in pediatrician.