Reticular dysgenesis

Known as: Immunoerythromyeloid Hypoplasia, De Vaal Disease, Severe combined immunodeficiency with leukopenia 
A rare severe combined immunodeficiency disorder characterized by congenital agranulocytosis, lymphoid tissue and thymic tissue hypoplasia, and… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1950-2017
024619502016

Papers overview

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2009
2009
Human severe combined immunodeficiencies (SCID) are phenotypically and genotypically heterogeneous diseases. Reticular dysgenesis… (More)
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2009
2009
Agenesis of the corpus callosum is associated with many human developmental syndromes. Key mechanisms regulating callosal… (More)
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2002
2002
Reticular dysgenesis is a very rare congenital immunodeficiency classified within the severe combined immunodeficiencies (SCID… (More)
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2000
2000
Reticular dysgenesis is a rare inherited immunodeficiency characterized by the lack of blood monocytes and neutrophils and low… (More)
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1999
1999
Reticular dysgenesis is a rare congenital disorder characterized by severe combined immunodeficiency and profound neutropenia… (More)
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Highly Cited
1997
Highly Cited
1997
OBJECTIVE To determine the relative frequencies of the different genetic forms of severe combined immunodeficiency (SCID) and… (More)
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1996
1996
We report two cases of reticular dysgenesis (RD) successfully treated by BMT utilizing T cell-depleted haploidentical marrow… (More)
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1985
1985
We report fatal reticular dysgenesis in a premature infant presenting with severely decreased blood and bone marrow granulocytes… (More)
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1983
1983
A male infant with reticular dysgenesis received a bone-marrow transplant from his HLA-identical brother. Severe graft-versus… (More)
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1976
1976
The hematologic and histologic features of two, nontwin, male siblings with severe combined immunodeficiency and variable… (More)
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