Congenital dyserythropoietic anemia type II

From WikiMD's WELLNESSPEDIA


Congenital dyserythropoietic anemia type II
Synonyms HEMPAS (Hereditary erythroblastic multinuclearity with positive acidified serum test)
Pronounce N/A
Specialty N/A
Symptoms Anemia, jaundice, splenomegaly, gallstones
Complications Iron overload, gallstones
Onset Childhood
Duration Lifelong
Types
Causes Genetic mutation in the SEC23B gene
Risks
Diagnosis Blood test, bone marrow biopsy, genetic testing
Differential diagnosis Other types of congenital dyserythropoietic anemia, hereditary spherocytosis
Prevention N/A
Treatment Blood transfusion, iron chelation therapy, splenectomy
Medication
Prognosis Variable, depending on severity
Frequency Rare
Deaths


- Congenital dyserythropoietic anemia type II (CDA II), or hereditary erythroblastic multinuclearity with positive acidified serum lysis test (HEMPAS) is a rare genetic anemia in humans characterized by hereditary erythroblastic multinuclearity with positive acidified serum lysis test. [[Category:Uncategorized

WikiMD logo

This article is a stub

You can help WikiMD by registering and expanding it with useful details, internal links, formatting, and categories.

Editing is available only to registered and verified users. WikiMD is a comprehensive, free health and wellness encyclopedia.


Medical Disclaimer: WikiMD is for informational purposes only and is not a substitute for professional medical advice. Content may be inaccurate or outdated and should not be used for diagnosis or treatment. Always consult your healthcare provider for medical decisions. Verify information with trusted sources such as CDC.gov and NIH.gov. By using this site, you agree that WikiMD is not liable for any outcomes related to its content. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.

Retrieved from "https://wikimd.org/index.php?title=Congenital_dyserythropoietic_anemia_type_II&oldid=6543418"