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About 138 results

ALLMedicine™ Hereditary Elliptocytosis Center

Research & Reviews  53 results

Hereditary Pyropoikilocytosis
https://emedicine.medscape.com/article/205843-overview

Aug 24th, 2021 - Practice Essentials Hereditary pyropoikilocytosis (HPP) is an autosomal recessive disorder of the red blood cell (RBC) membrane that is clinically related to, and is considered a subtype of, hereditary elliptocytosis (HE). HPP involves a functiona...

Hereditary Pyropoikilocytosis Clinical Presentation
https://emedicine.medscape.com/article/205843-clinical

Aug 24th, 2021 - History Hereditary pyropoikilocytosis (HPP) is considered the most severe type of hereditary elliptocytosis (HE) and manifests during infancy. HP is generally recognized when an infant or young child presents with a transfusion-dependent hemolytic...

Hereditary Pyropoikilocytosis
https://emedicine.medscape.com/article/205843-print

Aug 24th, 2021 - Practice Essentials Hereditary pyropoikilocytosis (HPP) is an autosomal recessive disorder of the red blood cell (RBC) membrane that is clinically related to, and is considered a subtype of, hereditary elliptocytosis (HE). HPP involves a functiona...

Hereditary Pyropoikilocytosis
http://emedicine.medscape.com/article/205843-overview

Aug 24th, 2021 - Practice Essentials Hereditary pyropoikilocytosis (HPP) is an autosomal recessive disorder of the red blood cell (RBC) membrane that is clinically related to, and is considered a subtype of, hereditary elliptocytosis (HE). HPP involves a functiona...

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Clinicaltrials.gov  2 results

Gall Bladder Status Among Children With Chronic Haemolytic Anemia
https://clinicaltrials.gov/ct2/show/NCT03533322

Jul 31st, 2018 - Gall bladder status among children with chronic haemolytic anemia attending to Assuit University Children Hospital Hemolysis is defined as the premature destruction of red blood cells (RBCs) (a shortened RBC life span). Anemia results when the rat...

A Novel Mutation of the Spectrin Gene
https://clinicaltrials.gov/ct2/show/NCT00723567

Feb 19th, 2009 - Mutations of spectrin (Sp) involving the Sp heterodimer self-association site (the I domain of Sp) represent the most common group of membrane skeletal defects in hereditary elliptocytosis (HE) and a closely related disorder, hereditary pyropoikil...

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