• Je něco špatně v tomto záznamu ?

Mosaicism for GJB1 mutation causes milder Charcot-Marie-Tooth X1 phenotype in a heterozygous man than in a manifesting heterozygous woman

I. Borgulová, R. Mazanec, I. Sakmaryová, M. Havlová, D. Safka Brožková, P. Seeman,

. 2013 ; 14 (3-4) : 189-95.

Jazyk angličtina Země Spojené státy americké

Typ dokumentu kazuistiky, časopisecké články, Research Support, N.I.H., Extramural

Perzistentní odkaz   https://www.medvik.cz/link/bmc14064073

Grantová podpora
NT11521 MZ0 CEP - Centrální evidence projektů

Digitální knihovna NLK
Plný text - Článek
Zdroj

E-zdroje Online Plný text

NLK ProQuest Central od 1997-05-01 do Před 1 rokem
Medline Complete (EBSCOhost) od 2004-02-01 do Před 1 rokem
Health & Medicine (ProQuest) od 1997-05-01 do Před 1 rokem
Psychology Database (ProQuest) od 1997-05-01 do Před 1 rokem

Charcot-Marie-Tooth (CMT) disease is a heterogeneous disorder of the peripheral nervous system that collectively affects approximately 1 in 2,500 individuals, thus making it the most common inherited neurologic disorder. X-linked inheritance may account for 10-20 % of CMT neuropathy. We report a Czech family with a 30-year-old woman affected by CMT since the age of 10 years, originally as an isolated case. Nerve conduction study (NCS) showed demyelinating neuropathy, and DNA testing revealed a novel heterozygous gap junction beta-1 protein (GJB1) mutation c.784_786delTA. The same mutation, but surprisingly in heterozygous state, was subsequently found in her subjectively healthy father and later also in one of her sisters but not in her two other sisters. NCS showed intermediate type of motor and sensory neuropathy in these two females manifesting heterozygotes and normal results in the other healthy sisters and one brother, all without the c.784_786delTA mutation. The father has a phenotype milder than his daughter and has only subclinical signs of CMT. The index female patient had normal karyotype 46, XX, and normal FISH for centromeric X chromosome. We concluded that the proband's father is a heterozygote due to the somatic mosaicism for the GJB1 mutation in his leukocytes (detected by DNA sequencing) and also in his germ cells as confirmed by the unexpectedly different genotypes in his four daughters. Quantitative analysis revealed a mutated signal in 25:75 allele proportion of mutated to healthy allele in the mosaic father. This study has important consequences for genetic counseling and prognosis in CMTX1 families.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc14064073
003      
CZ-PrNML
005      
20220613130549.0
007      
ta
008      
140704s2013 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1007/s10048-013-0368-7 $2 doi
035    __
$a (PubMed)23912496
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Borgulová, Irena, $u Centre for Medical Genetics and Reproductive Medicine GENNET, Prague, Czech Republic. i.eliasova@seznam.cz $d 1982- $7 xx0273859
245    10
$a Mosaicism for GJB1 mutation causes milder Charcot-Marie-Tooth X1 phenotype in a heterozygous man than in a manifesting heterozygous woman / $c I. Borgulová, R. Mazanec, I. Sakmaryová, M. Havlová, D. Safka Brožková, P. Seeman,
520    9_
$a Charcot-Marie-Tooth (CMT) disease is a heterogeneous disorder of the peripheral nervous system that collectively affects approximately 1 in 2,500 individuals, thus making it the most common inherited neurologic disorder. X-linked inheritance may account for 10-20 % of CMT neuropathy. We report a Czech family with a 30-year-old woman affected by CMT since the age of 10 years, originally as an isolated case. Nerve conduction study (NCS) showed demyelinating neuropathy, and DNA testing revealed a novel heterozygous gap junction beta-1 protein (GJB1) mutation c.784_786delTA. The same mutation, but surprisingly in heterozygous state, was subsequently found in her subjectively healthy father and later also in one of her sisters but not in her two other sisters. NCS showed intermediate type of motor and sensory neuropathy in these two females manifesting heterozygotes and normal results in the other healthy sisters and one brother, all without the c.784_786delTA mutation. The father has a phenotype milder than his daughter and has only subclinical signs of CMT. The index female patient had normal karyotype 46, XX, and normal FISH for centromeric X chromosome. We concluded that the proband's father is a heterozygote due to the somatic mosaicism for the GJB1 mutation in his leukocytes (detected by DNA sequencing) and also in his germ cells as confirmed by the unexpectedly different genotypes in his four daughters. Quantitative analysis revealed a mutated signal in 25:75 allele proportion of mutated to healthy allele in the mosaic father. This study has important consequences for genetic counseling and prognosis in CMTX1 families.
650    _2
$a dospělí $7 D000328
650    _2
$a Charcotova-Marieova-Toothova nemoc $x diagnóza $x genetika $7 D002607
650    _2
$a konexiny $x genetika $7 D017630
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a geny vázané na chromozom X $7 D050172
650    12
$a heterozygot $7 D006579
650    _2
$a lidé $7 D006801
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a lidé středního věku $7 D008875
650    12
$a mozaicismus $7 D009030
650    _2
$a periferní nervy $x patofyziologie $7 D010525
651    _2
$a Česká republika $7 D018153
655    _2
$a kazuistiky $7 D002363
655    _2
$a časopisecké články $7 D016428
655    _2
$a Research Support, N.I.H., Extramural $7 D052061
700    1_
$a Mazanec, Radim, $d 1959- $7 xx0037204 $u Department of Neurology, 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, Prague, Czech Republic
700    1_
$a Dolinová, Iva $7 xx0070781 $u Department of Child Neurology, 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, Prague, Czech Republic
700    1_
$a Havlová, Miluše, $d 1943-2022 $7 nlk19990073201 $u Department of Neurology, 1st Faculty of Medicine, Charles University in Prague and University General Hospital, Prague, Czech Republic
700    1_
$a Šafka-Brožková, Dana, $d 1981- $7 xx0100859 $u Department of Child Neurology, 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, Prague, Czech Republic
700    1_
$a Seeman, Pavel, $d 1966- $7 xx0037870 $u Centre for Medical Genetics and Reproductive Medicine GENNET, Prague, Czech Republic; Department of Child Neurology, 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, Prague, Czech Republic
773    0_
$w MED00005780 $t Neurogenetics $x 1364-6753 $g Roč. 14, č. 3-4 (2013), s. 189-95
856    41
$u https://pubmed.ncbi.nlm.nih.gov/23912496 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20140704 $b ABA008
991    __
$a 20220613130547 $b ABA008
999    __
$a ok $b bmc $g 1031557 $s 862805
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2013 $b 14 $c 3-4 $d 189-95 $i 1364-6753 $m Neurogenetics $n Neurogenetics $x MED00005780
GRA    __
$a NT11521 $p MZ0
LZP    __
$a Pubmed-20140704

Najít záznam

Citační ukazatele

Nahrávání dat ...

    Možnosti archivace