U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Autosomal recessive lymphoproliferative disease

MedGen UID:
1661274
•Concept ID:
C4749826
•
Disease or Syndrome
Synonyms: autosomal recessive lymphoproliferative disease; Autosomal recessive lymphoproliferative disease due to CD27 deficiency; CD27 deficiency; Combined immunodeficiency due to CD27 deficiency
SNOMED CT: Autosomal recessive lymphoproliferative disease (771309000)
Modes of inheritance:
Autosomal recessive inheritance
MedGen UID:
141025
•Concept ID:
C0441748
•
Intellectual Product
Source: Orphanet
A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in individuals with two pathogenic alleles, either homozygotes (two copies of the same mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele).
Autosomal recessive inheritance (Orphanet)
 
Monarch Initiative: MONDO:0016536
Orphanet: ORPHA238505

Definition

A rare combined T and B cell immunodeficiency with a predisposition to lymphoproliferative syndrome. It is characterised by persistent symptomatic Epstein-Barr viraemia and hypogammaglobulinaemia variably presenting with fever, lymphadenopathy and systemic inflammatory conditions including hepatitis, pneumonia and sepsis. It may be associated with lymphoma, haemophagocytic lymphohistiocytosis, and aplastic anaemia. [from SNOMEDCT_US]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVAutosomal recessive lymphoproliferative disease

Professional guidelines

PubMed

Agammaglobulinemia: Epidemiology, Pathogenesis, Clinical Phenotype, Diagnosis, Prognosis and Management.
Pashangzadeh S, Yazdani R, Nazari F, Azizi G, Abolhassani H, Aghamohammadi A
Endocr Metab Immune Disord Drug Targets 2020;20(9):1434-1447. doi: 10.2174/1871530320666200508114349. PMID: 32384040
Bladder Artery Embolization for Massive Hematuria Treatment in a Patient With Ataxia-Telangiectasia Acute Lymphoblastic Leukemia.
Bahadir A, Oguz Ş, Erduran E, Dinç H, Yalçin Cömert HS, Bahat Özdogan E, Kaya G
J Pediatr Hematol Oncol 2020 May;42(4):316-318. doi: 10.1097/MPH.0000000000001471. PMID: 30933018
Prenatal diagnosis and genetic analysis of X-linked immunodeficiency disorders.
Puck JM
Pediatr Res 1993 Jan;33(1 Suppl):S29-33; discussion S33-4. doi: 10.1203/00006450-199305001-00158. PMID: 8433872

Recent clinical studies

Etiology

H syndrome treated with Tocilizumab: two case reports and literature review.
Jacquot R, Jouret M, Valentin MG, Richard M, Jamilloux Y, Rousset F, Emile JF, Haroche J, Steinmüller L, Zekre F, Phan A, Belot A, Seve P
Front Immunol 2023;14:1061182. Epub 2023 Aug 11 doi: 10.3389/fimmu.2023.1061182. PMID: 37638031Free PMC Article
Clinical course and therapeutic implications for lymphoid malignancies in Nijmegen breakage syndrome.
Pastorczak A, Szczepanski T, Mlynarski W; International Berlin-Frankfurt-Munster (I-BFM) ALL host genetic variation working group
Eur J Med Genet 2016 Mar;59(3):126-32. Epub 2016 Jan 27 doi: 10.1016/j.ejmg.2016.01.007. PMID: 26826318
Gaucher disease and myeloma.
Ayto R, Hughes DA
Crit Rev Oncog 2013;18(3):247-68. doi: 10.1615/critrevoncog.2013006061. PMID: 23510067
Ig beta deficiency in humans.
Lougaris V, Ferrari S, Plebani A
Curr Opin Allergy Clin Immunol 2008 Dec;8(6):515-9. doi: 10.1097/ACI.0b013e328314b621. PMID: 18978465
Hemophagocytic lymphohistiocytosis and related disorders.
Filipovich AH
Curr Opin Allergy Clin Immunol 2006 Dec;6(6):410-5. doi: 10.1097/01.all.0000246626.57118.d9. PMID: 17088644

Diagnosis

Cystic fibrosis in children: A pediatric anesthesiologist's perspective.
Williamson DM, Sharma A
Paediatr Anaesth 2022 Feb;32(2):167-173. Epub 2022 Jan 10 doi: 10.1111/pan.14384. PMID: 34963200
Agammaglobulinemia: from X-linked to Autosomal Forms of Disease.
Cardenas-Morales M, Hernandez-Trujillo VP
Clin Rev Allergy Immunol 2022 Aug;63(1):22-35. Epub 2021 Jul 9 doi: 10.1007/s12016-021-08870-5. PMID: 34241796Free PMC Article
Hemophagocytic Lymphohistiocytosis: Clinical Presentations and Diagnosis.
Risma KA, Marsh RA
J Allergy Clin Immunol Pract 2019 Mar;7(3):824-832. Epub 2018 Dec 14 doi: 10.1016/j.jaip.2018.11.050. PMID: 30557712
ADA Deficiency: Evaluation of the Clinical and Laboratory Features and the Outcome.
Cagdas D, Gur Cetinkaya P, Karaatmaca B, Esenboga S, Tan C, Yılmaz T, Gümüş E, Barış S, Kuşkonmaz B, Ozgur TT, Bali P, Santisteban I, Orhan D, Yüce A, Cetinkaya D, Boztug K, Hershfield M, Sanal O, Tezcan İ
J Clin Immunol 2018 May;38(4):484-493. Epub 2018 May 9 doi: 10.1007/s10875-018-0496-9. PMID: 29744787
Gaucher disease and myeloma.
Ayto R, Hughes DA
Crit Rev Oncog 2013;18(3):247-68. doi: 10.1615/critrevoncog.2013006061. PMID: 23510067

Therapy

The same mutation in a family with adenosine deaminase 2 deficiency.
Sozeri B, Ercan G, Dogan OA, Yıldız J, Demir F, Doğanay L
Rheumatol Int 2021 Jan;41(1):227-233. Epub 2019 Sep 20 doi: 10.1007/s00296-019-04444-z. PMID: 31541281
Agammaglobulinemia: Epidemiology, Pathogenesis, Clinical Phenotype, Diagnosis, Prognosis and Management.
Pashangzadeh S, Yazdani R, Nazari F, Azizi G, Abolhassani H, Aghamohammadi A
Endocr Metab Immune Disord Drug Targets 2020;20(9):1434-1447. doi: 10.2174/1871530320666200508114349. PMID: 32384040
Common variable immune deficiency: Dissection of the variable.
Cunningham-Rundles C
Immunol Rev 2019 Jan;287(1):145-161. doi: 10.1111/imr.12728. PMID: 30565247Free PMC Article
Clinical course and therapeutic implications for lymphoid malignancies in Nijmegen breakage syndrome.
Pastorczak A, Szczepanski T, Mlynarski W; International Berlin-Frankfurt-Munster (I-BFM) ALL host genetic variation working group
Eur J Med Genet 2016 Mar;59(3):126-32. Epub 2016 Jan 27 doi: 10.1016/j.ejmg.2016.01.007. PMID: 26826318
Gaucher disease: haematological presentations and complications.
Thomas AS, Mehta A, Hughes DA
Br J Haematol 2014 May;165(4):427-40. Epub 2014 Mar 3 doi: 10.1111/bjh.12804. PMID: 24588457

Prognosis

Agammaglobulinemia: from X-linked to Autosomal Forms of Disease.
Cardenas-Morales M, Hernandez-Trujillo VP
Clin Rev Allergy Immunol 2022 Aug;63(1):22-35. Epub 2021 Jul 9 doi: 10.1007/s12016-021-08870-5. PMID: 34241796Free PMC Article
Agammaglobulinemia: Epidemiology, Pathogenesis, Clinical Phenotype, Diagnosis, Prognosis and Management.
Pashangzadeh S, Yazdani R, Nazari F, Azizi G, Abolhassani H, Aghamohammadi A
Endocr Metab Immune Disord Drug Targets 2020;20(9):1434-1447. doi: 10.2174/1871530320666200508114349. PMID: 32384040
Evaluation of B lymphocyte deficiencies.
Vickery JD, Michael CF, Lew DB
Cardiovasc Hematol Disord Drug Targets 2013 Aug;13(2):133-43. doi: 10.2174/1871529x11313020006. PMID: 23988001
Gaucher disease and myeloma.
Ayto R, Hughes DA
Crit Rev Oncog 2013;18(3):247-68. doi: 10.1615/critrevoncog.2013006061. PMID: 23510067
Chediak-Higashi syndrome.
Kaplan J, De Domenico I, Ward DM
Curr Opin Hematol 2008 Jan;15(1):22-9. doi: 10.1097/MOH.0b013e3282f2bcce. PMID: 18043242

Clinical prediction guides

Agammaglobulinemia: from X-linked to Autosomal Forms of Disease.
Cardenas-Morales M, Hernandez-Trujillo VP
Clin Rev Allergy Immunol 2022 Aug;63(1):22-35. Epub 2021 Jul 9 doi: 10.1007/s12016-021-08870-5. PMID: 34241796Free PMC Article
Evaluation of respiratory complications in patients with X-linked and autosomal recessive agammaglobulinemia.
Fekrvand S, Yazdani R, Olbrich P, Azizi G, Shirzadi R, Modaresi M, Sohani M, Delavari S, Kalantari A, Shariat M, Shafiei A, Lu N, Hassanpour G, Rahimi Hajiabadi M, Ashournia P, Razaghian A, Asgharyan M, Shahraki-Ghadimi Z, Rouhani R, Hoda Fallah F, Rezaei N, Abolhassani H, Aghamohammadi A
Pediatr Allergy Immunol 2020 May;31(4):405-417. Epub 2020 Mar 6 doi: 10.1111/pai.13228. PMID: 32058651
ADA Deficiency: Evaluation of the Clinical and Laboratory Features and the Outcome.
Cagdas D, Gur Cetinkaya P, Karaatmaca B, Esenboga S, Tan C, Yılmaz T, Gümüş E, Barış S, Kuşkonmaz B, Ozgur TT, Bali P, Santisteban I, Orhan D, Yüce A, Cetinkaya D, Boztug K, Hershfield M, Sanal O, Tezcan İ
J Clin Immunol 2018 May;38(4):484-493. Epub 2018 May 9 doi: 10.1007/s10875-018-0496-9. PMID: 29744787
A Comparison of Clinical and Immunologic Phenotypes in Familial and Sporadic Forms of Common Variable Immunodeficiency.
Valizadeh A, Yazdani R, Azizi G, Abolhassani H, Aghamohammadi A
Scand J Immunol 2017 Oct;86(4):239-247. doi: 10.1111/sji.12593. PMID: 28805315
Chediak-Higashi syndrome.
Kaplan J, De Domenico I, Ward DM
Curr Opin Hematol 2008 Jan;15(1):22-9. doi: 10.1097/MOH.0b013e3282f2bcce. PMID: 18043242

Recent systematic reviews

Purine Nucleoside Phosphorylase Deficient Severe Combined Immunodeficiencies: A Case Report and Systematic Review (1975-2022).
Habib Dzulkarnain SM, Hashim IF, Zainudeen ZT, Taib F, Mohamad N, Nasir A, Wan Ab Rahman WS, Ariffin H, Abd Hamid IJ
J Clin Immunol 2023 Oct;43(7):1623-1639. Epub 2023 Jun 16 doi: 10.1007/s10875-023-01532-5. PMID: 37328647
Clinical, Immunologic and Molecular Spectrum of Patients with Immunodeficiency, Centromeric Instability, and Facial Anomalies (ICF) Syndrome: A Systematic Review.
Kiaee F, Zaki-Dizaji M, Hafezi N, Almasi-Hashiani A, Hamedifar H, Sabzevari A, Shirkani A, Zian Z, Jadidi-Niaragh F, Aghamahdi F, Goudarzvand M, Yazdani R, Abolhassani H, Aghamohammadi A, Azizi G
Endocr Metab Immune Disord Drug Targets 2021;21(4):664-672. doi: 10.2174/1871530320666200613204426. PMID: 32533820

Supplemental Content

Table of contents

    Clinical resources

    Practice guidelines

    • PubMed
      See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the FAQ for details.
    • Bookshelf
      See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the FAQ for details.

    Consumer resources

    Reviews

    Related information

    • PMC Articles
      Related information in PubMed Central Links
    • PubMed
      Related literature resources in PubMed

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...