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LAMP2 exon-copy number variations in Danon disease heterozygote female probands: Infrequent or underdetected?
F. Majer, L. Piherova, M. Reboun, V. Stara, O. Pelak, P. Norambuena, V. Stranecky, A. Krebsova, H. Vlaskova, L. Dvorakova, S. Kmoch, T. Kalina, M. Kubanek, J. Sikora,
Language English Country United States
Document type Case Reports, Journal Article, Research Support, Non-U.S. Gov't
Grant support
GAUK 580716
Grantová Agentura, Univerzita Karlova - International
NCMG LM2015091, NPU I no. LO1604
Ministerstvo Školství, Mládeže a Tělovýchovy - International
AZV-MZ ČR 15-27682A, AZV-MZ ČR 15-33297A, RVO-VFN 64165/2012, VZ IKEM (00023001)
Ministerstvo Zdravotnictví České Republiky - International
PROGRESS Q26, PRVOUK P24
Univerzita Karlova v Praze - International
NV15-33297A
MZ0
CEP Register
NV15-27682A
MZ0
CEP Register
Digital library NLK
Full text - Article
Full text - Article
Source
NLK
Medline Complete (EBSCOhost)
from 2012-06-01 to 1 year ago
PubMed
30194816
DOI
10.1002/ajmg.a.40430
Knihovny.cz E-resources
- MeSH
- Child MeSH
- Adult MeSH
- Exons genetics MeSH
- Glycogen Storage Disease Type IIb genetics MeSH
- Heterozygote MeSH
- Humans MeSH
- Lysosomal-Associated Membrane Protein 2 genetics MeSH
- Adolescent MeSH
- Young Adult MeSH
- Family MeSH
- Pedigree MeSH
- Base Sequence MeSH
- DNA Copy Number Variations genetics MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
- Research Support, Non-U.S. Gov't MeSH
Danon disease (DD) is an X-linked disorder caused by mutations in the lysosomal-associated membrane protein 2 (LAMP2) gene (Xq24). DD is characterized by cognitive deficit, myopathy, and cardiomyopathy in male patients. The phenotype is variable and mitigated in females. The timely identification of de-novo LAMP2 mutated family members, many of whom are heterozygous females, remains critical for their treatment and family counseling. DD laboratory testing builds on minimally invasive quantification of the LAMP2 protein in white blood cells and characterization of the specific mutation. This integrative approach is particularly helpful when assessing suspect female heterozygotes. LAMP2 exon-copy number variations (eCNVs) were so far reported only in X-hemizygous male DD probands. In heterozygous female DD probands, the wild-type allele may hamper the identification of an eCNV even if it results in the complete abolition of LAMP2 transcription and/or translation. To document the likely underappreciated rate of occurrence and point out numerous potential pitfalls of detection of the LAMP2 eCNVs, we present the first two DD heterozygote female probands who harbor novel multi-exon LAMP2 deletions. Critical for counseling and recurrence prediction, we also highlight the need to search for somatic-germinal mosaicism in DD families.
References provided by Crossref.org
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