Literature DB >> 25663137

Variable phenotype of severe immunodeficiencies associated with RMRP gene mutations.

Winnie Ip1, H Bobby Gaspar, Robert Kleta, Estelle Chanudet, Chiara Bacchelli, Alison Pitts, Zohreh Nademi, E Graham Davies, Mary A Slatter, Persis Amrolia, Kanchan Rao, Paul Veys, Andrew R Gennery, Waseem Qasim.   

Abstract

PURPOSE: Mutations in RMRP primarily give rise to Cartilage Hair Hypoplasia (CHH), a highly diverse skeletal disorder which can be associated with severe immunodeficiency. Increased availability of RMRP mutation screening has uncovered a number of infants with significant immunodeficiency but only mild or absent skeletal features. We surveyed the clinical and immunological phenotype of children who have undergone allogeneic haematopoietic stem cell transplantation for this condition in the UK.
METHODS: Thirteen patients with confirmed RMRP mutations underwent allogeneic stem cell transplantation (SCT) at two nationally commissioned centres using a variety of donors and conditioning regimens. Records were retrospectively reviewed.
RESULTS: Median time from clinical presentation to diagnosis was 12 months (range 1 to 276 months), with three infants diagnosed with severe combined immunodeficiency (SCID) without radiographical manifestations of CHH. A total of 17 allogeneic procedures were performed on 13 patients including two stem-cell top-ups. The median age at transplant was 32.4 months (range 1.5 to 125 months). Of the eleven surviving patients, median follow-up was 50 months (range 21.6 to 168 months).
CONCLUSIONS: RMRP mutations can cause short stature and significant immunodeficiency which can be corrected by allogeneic SCT and the diagnosis should be considered even in the absence of skeletal manifestations.

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Year:  2015        PMID: 25663137     DOI: 10.1007/s10875-015-0135-7

Source DB:  PubMed          Journal:  J Clin Immunol        ISSN: 0271-9142            Impact factor:   8.317


  34 in total

1.  Mutations in the RNA component of RNase mitochondrial RNA processing might cause Omenn syndrome.

Authors:  Chaim M Roifman; Yiping Gu; Amos Cohen
Journal:  J Allergy Clin Immunol       Date:  2006-04       Impact factor: 10.793

2.  High-throughput multiplexed T-cell-receptor excision circle quantitative PCR assay with internal controls for detection of severe combined immunodeficiency in population-based newborn screening.

Authors:  Jacalyn L Gerstel-Thompson; Jonathan F Wilkey; Jennifer C Baptiste; Jennifer S Navas; Sung-Yun Pai; Kenneth A Pass; Roger B Eaton; Anne Marie Comeau
Journal:  Clin Chem       Date:  2010-07-21       Impact factor: 8.327

3.  Consequences of mutations in the non-coding RMRP RNA in cartilage-hair hypoplasia.

Authors:  Pia Hermanns; Alison A Bertuch; Terry K Bertin; Brian Dawson; Mark E Schmitt; Chad Shaw; Bernhard Zabel; Brendan Lee
Journal:  Hum Mol Genet       Date:  2005-10-27       Impact factor: 6.150

Review 4.  The molecular basis of the cartilage-hair hypoplasia-anauxetic dysplasia spectrum.

Authors:  Christian T Thiel; Anita Rauch
Journal:  Best Pract Res Clin Endocrinol Metab       Date:  2011-02       Impact factor: 4.690

5.  Worldwide mutation spectrum in cartilage-hair hypoplasia: ancient founder origin of the major70A-->G mutation of the untranslated RMRP.

Authors:  Maaret Ridanpää; Pertti Sistonen; Susanna Rockas; David L Rimoin; Outi Mäkitie; Ilkka Kaitila
Journal:  Eur J Hum Genet       Date:  2002-07       Impact factor: 4.246

6.  Extended follow-up of the Finnish cartilage-hair hypoplasia cohort confirms high incidence of non-Hodgkin lymphoma and basal cell carcinoma.

Authors:  Mervi Taskinen; Annamari Ranki; Eero Pukkala; Leila Jeskanen; Ilkka Kaitila; Outi Mäkitie
Journal:  Am J Med Genet A       Date:  2008-09-15       Impact factor: 2.802

7.  Newborn screening for severe combined immunodeficiency and T-cell lymphopenia in California: results of the first 2 years.

Authors:  Antonia Kwan; Joseph A Church; Morton J Cowan; Rajni Agarwal; Neena Kapoor; Donald B Kohn; David B Lewis; Sean A McGhee; Theodore B Moore; E Richard Stiehm; Matthew Porteus; Constantino P Aznar; Robert Currier; Fred Lorey; Jennifer M Puck
Journal:  J Allergy Clin Immunol       Date:  2013-07       Impact factor: 10.793

8.  RMRP mutations in Japanese patients with cartilage-hair hypoplasia.

Authors:  Eiji Nakashima; Akihiko Mabuchi; Kenichi Kashimada; Toshikazu Onishi; Junwei Zhang; Hirofumi Ohashi; Gen Nishimura; Shiro Ikegawa
Journal:  Am J Med Genet A       Date:  2003-12-15       Impact factor: 2.802

9.  Evolutionary comparison provides evidence for pathogenicity of RMRP mutations.

Authors:  Luisa Bonafé; Emmanouil T Dermitzakis; Sheila Unger; Cheryl R Greenberg; Belinda A Campos-Xavier; Andreas Zankl; Catherine Ucla; Stylianos E Antonarakis; Andrea Superti-Furga; Alexandre Reymond
Journal:  PLoS Genet       Date:  2005-10       Impact factor: 5.917

10.  Phenotypic variations of cartilage hair hypoplasia: granulomatous skin inflammation and severe T cell immunodeficiency as initial clinical presentation in otherwise well child with short stature.

Authors:  Liza J McCann; Jo McPartland; Dawn Barge; Lisa Strain; David Bourn; Eduardo Calonje; Julian Verbov; Andrew Riordan; George Kokai; Chris M Bacon; Michael Wright; Mario Abinun
Journal:  J Clin Immunol       Date:  2013-11-12       Impact factor: 8.317

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  7 in total

1.  Analysis of clinical and immunologic phenotype in a large cohort of children and adults with cartilage-hair hypoplasia.

Authors:  Svetlana Kostjukovits; Paula Klemetti; Helena Valta; Timi Martelius; Luigi D Notarangelo; Mikko Seppänen; Mervi Taskinen; Outi Mäkitie
Journal:  J Allergy Clin Immunol       Date:  2017-03-09       Impact factor: 10.793

2.  Abnormal Newborn Screening Follow-up for Severe Combined Immunodeficiency in an Amish Cohort with Cartilage-Hair Hypoplasia.

Authors:  Ethan M Scott; Sharat Chandra; Jinzhu Li; Eric D Robinette; Miraides F Brown; Olivia K Wenger
Journal:  J Clin Immunol       Date:  2020-01-06       Impact factor: 8.317

3.  Investigation of the causal etiology in a patient with T-B+NK+ immunodeficiency.

Authors:  Robert Sertori; Jian-Xin Lin; Esteban Martinez; Sadhna Rana; Andrew Sharo; Majid Kazemian; Uma Sunderam; Mark Andrake; Susan Shinton; Billy Truong; Roland M Dunbrack; Chengyu Liu; Rajgopol Srinivasan; Steven E Brenner; Christine M Seroogy; Jennifer M Puck; Warren J Leonard; David L Wiest
Journal:  Front Immunol       Date:  2022-07-29       Impact factor: 8.786

4.  Reduced Intensity Conditioning Allogeneic Transplant for SCID Associated with Cartilage Hair Hypoplasia.

Authors:  Taylor Fitch; Jack Bleesing; Rebecca A Marsh; Sharat Chandra
Journal:  J Clin Immunol       Date:  2022-07-15       Impact factor: 8.542

5.  Lymphomas in cartilage-hair hypoplasia - A case series of 16 patients reveals advanced stage DLBCL as the most common form.

Authors:  Hanna-Leena Kukkola; Pauliina Utriainen; Pasi Huttunen; Mervi Taskinen; Outi Mäkitie; Svetlana Vakkilainen
Journal:  Front Immunol       Date:  2022-09-23       Impact factor: 8.786

6.  A 30-Year Prospective Follow-Up Study Reveals Risk Factors for Early Death in Cartilage-Hair Hypoplasia.

Authors:  Svetlana Vakkilainen; Mervi Taskinen; Paula Klemetti; Eero Pukkala; Outi Mäkitie
Journal:  Front Immunol       Date:  2019-07-16       Impact factor: 7.561

7.  The Safety and Efficacy of Live Viral Vaccines in Patients With Cartilage-Hair Hypoplasia.

Authors:  Svetlana Vakkilainen; Iivari Kleino; Jarno Honkanen; Harri Salo; Leena Kainulainen; Michaela Gräsbeck; Eliisa Kekäläinen; Outi Mäkitie; Paula Klemetti
Journal:  Front Immunol       Date:  2020-08-11       Impact factor: 7.561

  7 in total

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