Also Known As
ATR syndrome linked to chromosome 16ATR syndrome, deletion typeATR-16 SyndromeATR-16 syndromeAlpha thalassemia-intellectual disability syndromeAlpha thalassemia-intellectual disability syndrome, deletion typeAlpha thalassemia-mental retardation syndromeAlpha-thalassemia-intellectual disability syndrome linked to chromosome type 16alpha thalassemia-intellectual disability syndrome, deletion typealpha thalassemia-retardation syndromealpha-thalassemia-intellectual disability syndrome linked to chromosome 16alpha-thalassemia/intellectual disability syndrome, deletion-typealpha-thalassemia/intellectual disability syndrome, type 1alpha-thalassemia/mental retardation syndrome, deletion-typealpha-thalassemia/mental retardation syndrome, type 1ALPHA-thalassemia/intellectual disability syndrome, chromosome 16-relatedALPHA-thalassemia/mental retardation syndrome, chromosome 16-relatedATR, deletion-typeAlpha-thalassemia/intellectual disability syndrome, deletion-typeAlpha-thalassemia/mental retardation syndrome, deletion-typeHaemoglobin H-related intellectual disabilityHaemoglobin H-related mental retardationHemoglobin H-related intellectual disabilityHemoglobin H-related mental retardationchromosome 16P deletion syndromeintellectual disability with Haemoglobin Hintellectual disability with Hemoglobin Hmental retardation with Haemoglobin Hmental retardation with Hemoglobin H
Definition
Alpha-thalassemia-intellectual deficit syndrome linked to chromosome 16 (ATR-16), a contiguous gene deletion syndrome, is a form of alpha-thalassemia characterized by microcytosis, hypochromia, normal hemoglobin (Hb) level or mild anemia, associated with developmental abnormalities.