-
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,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu kazuistiky, časopisecké články, Research Support, N.I.H., Extramural
Grantová podpora
NT11521
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Zdroj
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
- MeSH
- Charcotova-Marieova-Toothova nemoc diagnóza genetika MeSH
- dospělí MeSH
- geny vázané na chromozom X MeSH
- heterozygot * MeSH
- konexiny genetika MeSH
- lidé středního věku MeSH
- lidé MeSH
- mozaicismus * MeSH
- periferní nervy patofyziologie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- Research Support, N.I.H., Extramural MeSH
- Geografické názvy
- Česká republika MeSH
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