Immunologic Heterogeneity in 2 Cartilage-Hair Hypoplasia Patients With a Distinct Clinical Course
J. investig. allergol. clin. immunol
; 33(4): 263-270, 2023. tab, graf
Article
in English
| IBECS
| ID: ibc-223540
Responsible library:
ES1.1
Localization: ES15.1 - BNCS
ABSTRACT
Introduction:
Cartilage-hair hypoplasia (CHH) syndrome is a rare autosomal recessive syndrome associated with skeletal dysplasia, varying degrees of combined immunodeficiency (CID), short stature, hair hypoplasia, macrocytic anemia, increased risk of malignancies, and Hirschsprung disease.Purpose:
To provide clinical and immunological insights obtained from 2 unrelated patients who displayed clinical characteristics of CHH.Methods:
Two patients with suspected CHH syndrome due to skeletal dysplasia and immunodeficiency underwent an immunological and genetic work-up using flow cytometry, next-generation sequencing (NGS) of the immune repertoire, and Sanger sequencing to identify the underlying defects.Results:
Patient 1 presented with low birth weight and skeletal dysplasia. Newborn screening was suggestive of T-cell immunodeficiency, as T-cell receptor excision circle levels were undetectable. Both the T-cell receptor (TCR) Vß and TCR-g (TRG) repertoires were restricted, with evidence of clonal expansion. Genetic analysis identified compound heterozygous RMRP variants inherited from both parents. Patient 2 presented with recurrent lung and gastrointestinal infections, skeletal dysplasia, failure to thrive, and hepatomegaly. The polyclonal pattern of the TCRß repertoire was normal, with only slight overexpression of TCR-ßV20 and restricted expression of Vßs. TRG expressed a normal diverse repertoire, similar to that of the healthy control sample. Genetic analysis identified biallelic novel regulatory variants in RMRP. Both parents are carriers of this mutation.Conclusion:
Our findings demonstrate how the immunological work-up, supported by genetic findings, can dramatically change treatment and future outcome in patients with the same clinical syndrome (AU)
Full text:
Available
Collection:
National databases
/
Spain
Database:
IBECS
Main subject:
Hirschsprung Disease
/
Immunologic Deficiency Syndromes
Limits:
Humans
/
Infant
/
Infant, Newborn
Language:
English
Journal:
J. investig. allergol. clin. immunol
Year:
2023
Document type:
Article
Institution/Affiliation country:
Ambulatory Pediatrics/Palestinian Authority
/
Sheba Medical Center/Israel