Homocystinuria
Homocystinuria is an inherited metabolic disorder in which the body does not properly process certain amino acids, which causes their buildup in the blood and urine.
How it may present: It can be associated with vision changes, particular features in bones and joints, and effects on development; manifestations vary from person to person.
Why early detection matters: Identifying these disorders in a timely manner, through growth monitoring and screening programs, facilitates closer care.
Who treats it? The pediatrician guides the child's evaluation and coordination with areas specialized in metabolic diseases. When there are questions about development or screening results, it is advisable to discuss them with a professional who can interpret them.
Specialties that treat homocystinuria
Treatment by city
Doctors specialized in homocystinuria
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 homocystinuria?
Homocystinuria is an inherited metabolic disorder in which the body does not properly process certain amino acids, which causes their buildup in the blood and urine.
Which doctor treats homocystinuria?
Homocystinuria is usually treated by specialists in pediatrician.