Arterial hypertension in children with Williams-Beuren syndrome
<p>Williams-Beuren Syndrome (WBS) is a multisystemic disorder with prevalence of 1/7500 [1], affects both genders equally and it is caused by a microdeletion of 26-28 genes, including elastin and NCF1 genes, of the chromosome region 7q11.23 [1,2]. The disease is transmitted in an autosomal dom...
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Archives of Clinical Nephrology - Peertechz Publications,
2020-11-27.
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|---|---|---|---|
| 001 | peertech__10_17352_acn_000044 | ||
| 042 | |a dc | ||
| 100 | 1 | 0 | |a Novo Marta |e author |
| 700 | 1 | 0 | |a Loureiro Marília |e author |
| 700 | 1 | 0 | |a Rocha Liliana |e author |
| 245 | 0 | 0 | |a Arterial hypertension in children with Williams-Beuren syndrome |
| 260 | |b Archives of Clinical Nephrology - Peertechz Publications, |c 2020-11-27. | ||
| 520 | |a <p>Williams-Beuren Syndrome (WBS) is a multisystemic disorder with prevalence of 1/7500 [1], affects both genders equally and it is caused by a microdeletion of 26-28 genes, including elastin and NCF1 genes, of the chromosome region 7q11.23 [1,2]. The disease is transmitted in an autosomal dominant fashion, but almost all cases are the result of de novo mutations [1]. </p> | ||
| 540 | |a Copyright © Novo Marta et al. | ||
| 546 | |a en | ||
| 655 | 7 | |a Short Communication |2 local | |
| 856 | 4 | 1 | |u https://doi.org/10.17352/acn.000044 |z Connect to this object online. |