Reticular dysgenesis

Common Name(s)

Reticular dysgenesis

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Reticular dysgenesis" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Reticular dysgenesis" returned 7 free, full-text research articles on human participants. First 3 results:

Reticular dysgenesis: international survey on clinical presentation, transplantation, and outcome.
 

Author(s): Manfred Hoenig, Chantal Lagresle-Peyrou, Ulrich Pannicke, Luigi D Notarangelo, Fulvio Porta, Andrew R Gennery, Mary Slatter, Morton J Cowan, Polina Stepensky, Hamoud Al-Mousa, Daifulah Al-Zahrani, Sung-Yun Pai, Waleed Al Herz, Hubert B Gaspar, Paul Veys, Koichi Oshima, Kohsuke Imai, Hiromasa Yabe, Lenora M Noroski, Nico M Wulffraat, Karl-Walter Sykora, Pere Soler-Palacin, Hideki Muramatsu, Mariam Al Hilali, Despina Moshous, Klaus-Michael Debatin, Catharina Schuetz, Eva-Maria Jacobsen, Ansgar S Schulz, Klaus Schwarz, Alain Fischer, Wilhelm Friedrich, Marina Cavazzana,

Journal: Blood. 2017 05;129(21):2928-2938.

 

Reticular dysgenesis (RD) is a rare congenital disorder defined clinically by the combination of severe combined immunodeficiency (SCID), agranulocytosis, and sensorineural deafness. Mutations in the gene encoding adenylate kinase 2 were identified to cause the disorder. Hematopoietic ...

Last Updated: 31 Dec 1969

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First reported case of Omenn syndrome in a patient with reticular dysgenesis.
 

Author(s): Lauren A Henderson, Francesco Frugoni, Gregory Hopkins, Waleed Al-Herz, Katja Weinacht, Anne Marie Comeau, Francisco A Bonilla, Luigi D Notarangelo, Sung-Yun Pai

Journal: J. Allergy Clin. Immunol.. 2013 Apr;131(4):1227-30, 1230.e1-3.

 

Last Updated: 31 Dec 1969

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Reticular dysgenesis: HLA non-identical bone marrow transplants in a series of 10 patients.
 

Author(s): Y Bertrand, S M Müller, J L Casanova, G Morgan, A Fischer, W Friedrich

Journal: Bone Marrow Transplant.. 2002 May;29(9):759-62.

 

Reticular dysgenesis is a very rare congenital immunodeficiency classified within the severe combined immunodeficiencies (SCID) and characterized by impairment of both lymphoid and myeloid cell development. We report our experience in 10 patients with RD, treated between 1979 and ...

Last Updated: 31 Dec 1969

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Reticular dysgenesis" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

Natural History Study of SCID Disorders
 

Status: Recruiting

Condition Summary: SCID; Leaky SCID; Omenn Syndrome; Reticular Dysgenesis; ADA Deficiency; XSCID

 

Last Updated: 10 Oct 2017

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Patients Treated for SCID (1968-Present)
 

Status: Recruiting

Condition Summary: SCID; ADA-SCID; XSCID; Leaky SCID; Omenn Syndrome; Reticular Dysgenesis

 

Last Updated: 7 Nov 2017

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Allogeneic Hematopoietic Stem Cell Transplant for Patients With Primary Immune Deficiencies
 

Status: Recruiting

Condition Summary: SCID; Omenn's Syndrome; Reticular Dysgenesis; Wiskott-Aldrich Syndrome; Bare Lymphocyte Syndrome; Common Variable Immunodeficiency; Chronic Granulomatous Disease; CD40 Ligand Deficiency; Hyper IgM Syndrome; X-linked Lymphoproliferative Disease; Hemophagocytic Lymphohistiocytosis; Griscelli Syndrome; Chediak-Higashi Syndrome; Langerhan's Cell Histiocytosis

 

Last Updated: 25 Sep 2018

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