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Familial erythrocytosis

Known as: ERYTHROCYTOSIS, PRIMARY FAMILIAL, Erythrocytosis autosomal dominant benign, PFCP 
Polycythemia that occurs in groups of related individuals.
National Institutes of Health

Related topics

Related topics

18 relations
Autosomal dominant inheritanceCoronary Artery DiseaseDizzinessDyspnea on exertion

Broader (3)

Hematological DiseasePolycythemiasecondary polycythemia

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2011
Highly Cited
2011
Disruption of the ASXL1 gene is frequent in primary, post-essential thrombocytosis and post-polycythemia vera myelofibrosis, but not essential thrombocytosis or polycythemia vera: analysis of…
Background The myeloproliferative neoplasms, essential thrombocytosis, polycythemia vera and primary myelofibrosis, share the… 
2011
2011
Mutations galore in myeloproliferative neoplasms: Would the real Spartacus please stand up?
Mutations galore in myeloproliferative neoplasms: Would the real Spartacus please stand up? 
2010
2010
Hereditary myeloproliferative disorders
Hereditary forms of myeloproliferative disorders (MPD) can be divided into two broad categories. First, inherited syndromes that… 
2007
2007
Molecular genetic analyses in familial and sporadic congenital primary erythrocytosis.
Dominant mutations in the erythropoietin receptor (EPOR) gene account for only about 15% of cases of primary congenital… 
Review
2005
Review
2005
Lessons from familial myeloproliferative disorders.
By definition, myeloproliferative disorders (MPDs) are caused by an acquired somatic mutation of a hematopoietic progenitor/stem… 
Review
2000
Review
2000
Congenital and inherited polycythemia.
Absolute polycythemia is a condition with increased red blood cell mass. There are a number of primary and secondary polycythemic… 
1997
1997
Losartan, an angiotensin-II receptor antagonist, reduces hematocrits in kidney transplant recipients with posttransplant erythrocytosis.
BACKGROUND Posttransplant erythrocytosis (PTE) occurs in 10-15% of patients with a well-functioning kidney transplant and is… 
1980
1980
Congenital Erythrocytosis: a New Form Associated with an Erythropoietin‐dependent Mechanism
Three patients with probable congenital erythrocytosis were studied to determine the role of erythropoietin (ESF) in their… 
1977
1977
Erythropoiesis in familial erythrocytosis.
We found primary erythrocytosis in two male siblings with hematologically normal parents. To clarify the abnormalities in… 
1967
1967
Polycythemia vera with Ph-1 chromosomes in two brothers.
Two brothers with polycythemia rubra vera have been studied: one before treatment and one after many years of treatment. Direct… 
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