thalassemia
hereditary disorder of hemoglobin synthesis
- symptoms: anemia, jaundice, splenomegaly,
hemosiderosis,
cardiomegaly, rodent-like face, big head
- erythroid hyperplasia
=> increased medullary pressure
=> atrophy of cortical
and cancellous bone
- shafts flatten then become convex
- "hair-on-end" skull
- "honeycomb trabecular bone"
In puberty, peripheral manifestations regress as inactive yellow marrow
replaces active red marrow. Thus the skull, spine and pelvis demonstrate
the most severe changes in adulthood.
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© 2002, C.E. Kahn, Jr.
2002-04-18