-
Je něco špatně v tomto záznamu ?
The age dependent progression of Hajdu-Cheney syndrome in two families
J. Jirečková, M. Magner, L. Lambert, A. Baxová, A. Leiská, L. Kopečková, L. Fajkusová, J. Zeman
Jazyk angličtina Země Česko
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 2012
Medline Complete (EBSCOhost)
od 2012-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2013
- MeSH
- dítě MeSH
- Hajdu-Cheney syndrom * komplikace patologie MeSH
- kostní denzita MeSH
- lidé MeSH
- mladiství MeSH
- osteoporóza * etiologie MeSH
- prognóza MeSH
- progrese nemoci MeSH
- senioři MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- mladiství MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
Hajdu-Cheney syndrome (HCS) is a rare multi-system disease with autosomal dominant inheritance and skeletal involvement, resulting mostly in craniofacial dysmorphy with mid-face hypoplasia, dental anomalies, short stature, scoliosis, shortening of the digits and nail beds, acro-osteolysis and osteoporosis. We report the progression of clinical and radiographic findings in five patients with Hajdu-Cheney syndrome from two families. A custom capture array designed to capture exons and adjacent intron sequences of 230 selected genes were used for molecular analyses, and the pathogenic variants identified were confirmed by PCR and Sanger sequencing. In both families we observed age-dependent changes in the disease, with a progression of pain in older patients, a shortening of digits and nail beds on both the hands and feet, kyphoscoliosis and the persistence of Wormian bones in lambdoid sutures. Molecular analyses performed in two patients revealed that they are heterozygotes for a c.6255T>A (p.Cys2085*) variant in the NOTCH2 gene, resulting in a premature stop-codon. Bone mineral density (Z-score < -2) did not improved in a girl treated with calcium and vitamin D supplementation during childhood and bisphosphonate during adolescence. Hajdu-Cheney syndrome is a slowly progressive disease with a frequently unfavourable prognosis in elderly patients, especially for the development of dental anomalies, osteoporosis and the progression of skeletal complications requiring orthopedic surgeries.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc19015101
- 003
- CZ-PrNML
- 005
- 20190430145018.0
- 007
- ta
- 008
- 190423s2018 xr a f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.14712/23362936.2019.3 $2 doi
- 035 __
- $a (PubMed)30779700
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Jirečková, Jitka $u Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic $7 xx0231717
- 245 14
- $a The age dependent progression of Hajdu-Cheney syndrome in two families / $c J. Jirečková, M. Magner, L. Lambert, A. Baxová, A. Leiská, L. Kopečková, L. Fajkusová, J. Zeman
- 520 9_
- $a Hajdu-Cheney syndrome (HCS) is a rare multi-system disease with autosomal dominant inheritance and skeletal involvement, resulting mostly in craniofacial dysmorphy with mid-face hypoplasia, dental anomalies, short stature, scoliosis, shortening of the digits and nail beds, acro-osteolysis and osteoporosis. We report the progression of clinical and radiographic findings in five patients with Hajdu-Cheney syndrome from two families. A custom capture array designed to capture exons and adjacent intron sequences of 230 selected genes were used for molecular analyses, and the pathogenic variants identified were confirmed by PCR and Sanger sequencing. In both families we observed age-dependent changes in the disease, with a progression of pain in older patients, a shortening of digits and nail beds on both the hands and feet, kyphoscoliosis and the persistence of Wormian bones in lambdoid sutures. Molecular analyses performed in two patients revealed that they are heterozygotes for a c.6255T>A (p.Cys2085*) variant in the NOTCH2 gene, resulting in a premature stop-codon. Bone mineral density (Z-score < -2) did not improved in a girl treated with calcium and vitamin D supplementation during childhood and bisphosphonate during adolescence. Hajdu-Cheney syndrome is a slowly progressive disease with a frequently unfavourable prognosis in elderly patients, especially for the development of dental anomalies, osteoporosis and the progression of skeletal complications requiring orthopedic surgeries.
- 650 _2
- $a mladiství $7 D000293
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a kostní denzita $7 D015519
- 650 _2
- $a dítě $7 D002648
- 650 _2
- $a progrese nemoci $7 D018450
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 12
- $a Hajdu-Cheney syndrom $x komplikace $x patologie $7 D031845
- 650 _2
- $a lidé $7 D006801
- 650 12
- $a osteoporóza $x etiologie $7 D010024
- 650 _2
- $a prognóza $7 D011379
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Magner, Martin $u Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic $7 xx0084624
- 700 1_
- $a Lambert, Lukáš $u Department of Radiology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic $7 xx0145830
- 700 1_
- $a Baxová, Alice $u Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic $7 xx0088382
- 700 1_
- $a Leiská, Alena $u Department of Radiology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic $7 xx0236058
- 700 1_
- $a Kopečková, Lenka $u Centre of Molecular Biology and Gene Therapy, Masaryk University in Brno and University Hospital Brno, Brno, Czech Republic $7 xx0239996
- 700 1_
- $a Fajkusová, Lenka, $u Centre of Molecular Biology and Gene Therapy, Masaryk University in Brno and University Hospital Brno, Brno, Czech Republic $d 1963- $7 xx0062747
- 700 1_
- $a Zeman, Jiří, $u Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic $d 1950- $7 skuk0001517
- 773 0_
- $w MED00013414 $t Prague medical report $x 1214-6994 $g Roč. 119, č. 4 (2018), s. 156-164
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/30779700 $y Pubmed
- 856 41
- $u https://pmr.lf1.cuni.cz/media/pdf/pmr_2018119040156.pdf $y plný text volně přístupný
- 910 __
- $a ABA008 $b A 7 $c 1071 $y 4 $z 0
- 990 __
- $a 20190423 $b ABA008
- 991 __
- $a 20190430125802 $b ABA008
- 999 __
- $a ok $b bmc $g 1399648 $s 1053500
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2018 $b 119 $c 4 $d 156-164 $i 1214-6994 $m Prague Medical Report $n Prague Med. Rep. $x MED00013414
- LZP __
- $b NLK118 $a Pubmed-20190423