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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,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu kazuistiky, časopisecké články, práce podpořená grantem
Grantová podpora
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 - Centrální evidence projektů
NV15-27682A
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Plný text - Článek
Zdroj
NLK
Medline Complete (EBSCOhost)
od 2012-06-01 do Před 1 rokem
PubMed
30194816
DOI
10.1002/ajmg.a.40430
Knihovny.cz E-zdroje
- MeSH
- dítě MeSH
- dospělí MeSH
- exony genetika MeSH
- glykogenóza typu IIb genetika MeSH
- heterozygot MeSH
- lidé MeSH
- membránový protein 2 asociovaný s lyzozomy genetika MeSH
- mladiství MeSH
- mladý dospělý MeSH
- rodina MeSH
- rodokmen MeSH
- sekvence nukleotidů MeSH
- variabilita počtu kopií segmentů DNA genetika MeSH
- Check Tag
- dítě MeSH
- dospělí MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- práce podpořená grantem 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.
Citace poskytuje Crossref.org
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