Hemoglobinopathies are a group of inherited blood diseases caused by genetic disorders that modify the molecular structure of hemoglobin. For the early diagnosis of these diseases it is important to do a newborn screening with biochemical and genetic studies. Moreover, the latter are essential for genetic counseling in carriers for future pregnancies and prenatal diagnosis.
Biomedical Diagnostic Center (CDB)
Villarroel, 170 · 08036 Barcelona
Tel: +34 93 227 54 64 · Fax: +34 93 227 98 75 · atencdb(ELIMINAR)@clinic.cat · www.hospitalclinic.org