Hemoglobin H disease

  (Redirected from Hemoglobin H)

Hemoglobin H disease is a type of alpha thalassemia caused by impaired production of three of the four alpha globins, coded by genes HBA1 and HBA2.[1]

Hemoglobin H disease
Other namesAlpha-thalassemia intermedia
SpecialtyHematology

ReferencesEdit

  1. ^ "Pathophysiology of alpha thalassemia". www.uptodate.com. Retrieved 2016-08-30.

External linksEdit

Classification
External resources