Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations.
Cell Line
Child, Preschool
DNA Mutational Analysis
Disease Management
Female
Forkhead Transcription Factors
/ chemistry
Genetic Association Studies
Genetic Loci
Genetic Predisposition to Disease
Hematopoietic Stem Cell Transplantation
Heterozygote
High-Throughput Nucleotide Sequencing
Homozygote
Humans
Male
Models, Molecular
Molecular Conformation
Mutation
Pedigree
Phenotype
Severe Combined Immunodeficiency
/ diagnosis
Structure-Activity Relationship
Treatment Outcome
EBV-related lymphoproliferative disease
FOXN1
Nude SCID
Omenn syndrome
alopecia
compound heterozygous
heterozygous
homozygous
nail dystrophy
Journal
Journal of clinical immunology
ISSN: 1573-2592
Titre abrégé: J Clin Immunol
Pays: Netherlands
ID NLM: 8102137
Informations de publication
Date de publication:
05 2021
05 2021
Historique:
received:
21
07
2020
accepted:
06
01
2021
pubmed:
20
1
2021
medline:
21
1
2022
entrez:
19
1
2021
Statut:
ppublish
Résumé
Human nude SCID is a rare autosomal recessive inborn error of immunity (IEI) characterized by congenital athymia, alopecia, and nail dystrophy. Few cases have been reported to date. However, the recent introduction of newborn screening for IEIs and high-throughput sequencing has led to the identification of novel and atypical cases. Moreover, immunological alterations have been recently described in patients carrying heterozygous mutations. The aim of this paper is to describe the extended phenotype associated with FOXN1 homozygous, compound heterozygous, or heterozygous mutations. We collected clinical and laboratory information of a cohort of 11 homozygous, 2 compound heterozygous, and 5 heterozygous patients with recurrent severe infections. All, except one heterozygous patient, had signs of CID or SCID. Nail dystrophy and alopecia, that represent the hallmarks of the syndrome, were not always present, while almost 50% of the patients developed Omenn syndrome. One patient with hypomorphic compound heterozygous mutations had a late-onset atypical phenotype. A SCID-like phenotype was observed in 4 heterozygous patients coming from the same family. A spectrum of clinical manifestations may be associated with different mutations. The severity of the clinical phenotype likely depends on the amount of residual activity of the gene product, as previously observed for other SCID-related genes. The severity of the manifestations in this heterozygous family may suggest a mechanism of negative dominance of the specific mutation or the presence of additional mutations in noncoding regions.
Identifiants
pubmed: 33464451
doi: 10.1007/s10875-021-00967-y
pii: 10.1007/s10875-021-00967-y
pmc: PMC8068652
doi:
Substances chimiques
Forkhead Transcription Factors
0
Whn protein
0
Types de publication
Journal Article
Multicenter Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
756-768Subventions
Organisme : Medical Research Council
ID : MR/S036407/1
Pays : United Kingdom
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