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Page 1
Wiedemann-Rautenstrauch syndrome: A phenotype analysis.
Paolacci S, Bertola D, Franco J, Mohammed S, Tartaglia M, Wollnik B, Hennekam RC. Paolacci S, et al. Am J Med Genet A. 2017 Jul;173(7):1763-1772. doi: 10.1002/ajmg.a.38246. Epub 2017 Apr 26. Am J Med Genet A. 2017. PMID: 28447407
Wiedemann-Rautenstrauch syndrome (WRS) is a neonatal progeroid disorder characterized by growth retardation, lipodystrophy, a distinctive face, and dental anomalies. ...
Wiedemann-Rautenstrauch syndrome (WRS) is a neonatal progeroid disorder characterized by growth retardation, lipodystro …
Wiedemann-Rautenstrauch syndrome.
Toriello HV. Toriello HV. J Med Genet. 1990 Apr;27(4):256-7. doi: 10.1136/jmg.27.4.256. J Med Genet. 1990. PMID: 2325106 Free PMC article. No abstract available.
The neonatal progeroid syndrome (Wiedemann-Rautenstrauch): a model for the study of human aging?
Arboleda G, Ramírez N, Arboleda H. Arboleda G, et al. Exp Gerontol. 2007 Oct;42(10):939-43. doi: 10.1016/j.exger.2007.07.004. Epub 2007 Jul 19. Exp Gerontol. 2007. PMID: 17728088 Review.
The Wiedemann-Rautenstrauch syndrome (WRS) characterises a premature aging syndrome in which several features of human aging are apparent at birth therefore allowing their grouping as a neonatal progeroid condition. ...
The Wiedemann-Rautenstrauch syndrome (WRS) characterises a premature aging syndrome in which several features of human …
Wiedemann-Rautenstrauch syndrome prenatal diagnosis.
Becerra CH, Contreras-García GA, Perez Vera LA, Díaz-Martínez LA, Beltran Avendaño MA, Salazar Martínez HA. Becerra CH, et al. J Perinatol. 2014 Dec;34(12):954-6. doi: 10.1038/jp.2014.156. J Perinatol. 2014. PMID: 25421132 No abstract available.
Wiedemann-Rautenstrauch syndrome in an Indian patient with biallelic pathogenic variants in POLR3A.
Majethia P, Girisha KM. Majethia P, et al. Am J Med Genet A. 2021 May;185(5):1602-1605. doi: 10.1002/ajmg.a.62115. Epub 2021 Feb 8. Am J Med Genet A. 2021. PMID: 33559318
Wiedemann-Rautenstrauch syndrome (WRS; MIM# 264090) is a rare neonatal progeroid disorder resulting from biallelic pathogenic variants in the POLR3A. ...
Wiedemann-Rautenstrauch syndrome (WRS; MIM# 264090) is a rare neonatal progeroid disorder resulting from biallelic path …
A Case of Wiedemann-Rautenstrauch Syndrome With Fatal Hyperkalemic Renal Faliure.
Ghamry MA, Salah R, Galal EI, Henin S, Dobs M. Ghamry MA, et al. Cureus. 2022 Sep 19;14(9):e29320. doi: 10.7759/cureus.29320. eCollection 2022 Sep. Cureus. 2022. PMID: 36159344 Free PMC article.
Wiedemann-Rautenstrauch Syndrome (WRS), also known as neonatal progeroid syndrome, is an extremely rare genetic syndrome characterized by a senile appearance at birth with multiple complex symptoms. ...
Wiedemann-Rautenstrauch Syndrome (WRS), also known as neonatal progeroid syndrome, is an extremely rare genetic syndrom …
Neonatal progeroid syndrome (Wiedemann-Rautenstrauch syndrome): report of three affected sibs.
Arboleda G, Morales LC, Quintero L, Arboleda H. Arboleda G, et al. Am J Med Genet A. 2011 Jul;155A(7):1712-5. doi: 10.1002/ajmg.a.34019. Epub 2011 Jun 10. Am J Med Genet A. 2011. PMID: 21671373 Review.
The Wiedemann-Rautenstrauch syndrome (WRS) (OMIM 264090) is a rare progeroid entity. ...
The Wiedemann-Rautenstrauch syndrome (WRS) (OMIM 264090) is a rare progeroid entity. ...
Further delineation of Wiedemann-Rautenstrauch syndrome linked with POLR3A.
Khan A, Al Shamsi B, Al Shehhi M, Kashgari AA, Al Balushi A, Al Dihan FA, Alghamdi MA, Manal A, González-Álvarez AC, Arold ST, Eyaid W. Khan A, et al. Mol Genet Genomic Med. 2024 Mar;12(3):e2274. doi: 10.1002/mgg3.2274. Epub 2024 Feb 13. Mol Genet Genomic Med. 2024. PMID: 38348603 Free PMC article.
Wiedemann-Rautenstrauch Syndrome (WRS; MIM 264090) is an extremely rare and highly heterogeneous syndrome that is inherited in a recessive fashion. ...
Wiedemann-Rautenstrauch Syndrome (WRS; MIM 264090) is an extremely rare and highly heterogeneous syndrome that is inher …
Wiedemann-Rautenstrauch syndrome: first Indian case.
Pandey M, Gupta N, Kabra M, Kumar A, Datta V, Saili A. Pandey M, et al. Indian J Pediatr. 2011 Dec;78(12):1552-5. doi: 10.1007/s12098-011-0480-3. Epub 2011 Jun 1. Indian J Pediatr. 2011. PMID: 21630068
Wiedemann-Rautenstrauch syndrome, also known as neonatal progeroid syndrome (NPS), is an extremely rare genetic disorder characterised by an aged appearance at birth. About thirty cases have been reported in the literature. The authors report first Indian bab …
Wiedemann-Rautenstrauch syndrome, also known as neonatal progeroid syndrome (NPS), is an extremely rare genetic disorde …
64 results