An incontinentia pigmenti family with deletion in both NEMO gene and pseudogene DeltaNEMO.
- Author:
Guolong ZHANG
1
;
Hejian SHI
;
Xufeng DU
;
Minhua SHAO
;
Qing ZHOU
Author Information
- Publication Type:Journal Article
- MeSH: Adolescent; Child; Electrophoresis; Exons; genetics; Family; Female; Humans; I-kappa B Kinase; genetics; Incontinentia Pigmenti; genetics; Infant; Male; Pseudogenes; genetics; Sequence Deletion
- From: Chinese Journal of Medical Genetics 2008;25(5):573-575
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo detect the genomic deletion mutation in the NEMO gene of a family with incontinentia pigmenti (IP; MIM 308310).
METHODSA pedigree of IP was investigated. By using long PCR, the Delta4-10 deletion in NEMO gene was tested with specific primers In2/JF3R, and Delta4-10 deletion in pseudogene DeltaNEMO was investigated with primers Rev-2/JF3R. NEMO gene of 80 normal controls was also tested.
RESULTSThe deletion of exons 4-10 in both NEMO gene and the pseudogene DeltaNEMO was detected in all the patients in the family, but was not found in the normal individuals in this IP family and 80 unrelated controls.
CONCLUSIONThe study showed that the family with IP, which showed anticipation, was caused by NEMODelta4-10 deletion in the NEMO gene. Long PCR analysis is proven to be an efficient tool for identification of NEMO rearrangements. It could provide useful information for the genetic counseling of the family involved.
