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81258 - syndrome, HbH disease), gene analysis; known familial variant

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Procedure / Servicesyndrome, HbH disease), gene analysis; known familial variant
Procedure / Service Description

for attenuation correction and anatomical localization imaging; limited area (eg, chest, - 81257 Thai, Filipino, Mediterranean, alpha3.7, alpha4.2, alpha20.5, Constant Spring) HBA1/HBA2 (alpha globin 1 and alpha globin 2) (eg, alpha thalassemia, Hb Bart hydrops fetalis 81258 syndrome, HbH disease), gene analysis; known familial variant HBA1/HBA2 (alpha globin 1 and alpha globin 2) (eg, alpha thalassemia, Hb Bart hydrops fetalis 81259 syndrome, HbH disease), gene analysis; full gene sequence

Likely documents
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