<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Hemoglobinopathies on Leukoformula</title><link>https://www.leukoformula.com/en/tags/gemoglobinopatii/</link><description>Recent content in Hemoglobinopathies on Leukoformula</description><generator>Hugo</generator><language>en-US</language><lastBuildDate>Mon, 28 Aug 2023 12:52:36 +0300</lastBuildDate><atom:link href="https://www.leukoformula.com/en/tags/gemoglobinopatii/feed.xml" rel="self" type="application/rss+xml"/><item><title>Erythrocyte Morphology in Thalassemia and Hemoglobinopathies</title><link>https://www.leukoformula.com/en/post/morfologiya-eritrocitov-pri-talassemiyah-i-13067/</link><pubDate>Mon, 28 Aug 2023 12:52:36 +0300</pubDate><guid>https://www.leukoformula.com/en/post/morfologiya-eritrocitov-pri-talassemiyah-i-13067/</guid><description>&lt;p>🔬Working in the Mediterranean region, I encounter thalassemias and pathological hemoglobins in practice, which I only saw in atlases in Russia. I&amp;rsquo;ll share my personal collection.&lt;/p>
&lt;ol>
&lt;li>B-thalassemia major
Severe changes in the erythroid lineage:
Anisocytosis and aniso-chromia of erythrocytes,
Target cells,
Normoblasts,
Basophilic stippling,
Pappenheimer bodies,
Howell-Jolly bodies&lt;/li>
&lt;li>B-thalassemia minor
Very minor erythrocyte changes:
Hypochromia and occasional target cells.&lt;/li>
&lt;li>Sickle cell anemia (Hemoglobinopathy S)
Sickle cells&lt;/li>
&lt;li>Hemoglobinopathy C
Characteristic crystals of pathological hemoglobin C in erythrocytes.&lt;/li>
&lt;li>Hemoglobinopathy E
A migrant worker from Thailand.
Almost all erythrocytes are target cells.&lt;/li>
&lt;/ol>
&lt;p>❓Does anyone know why there is no need to present a blood picture of Alpha-thalassemia?&lt;/p></description></item></channel></rss>