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272 results

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Page 1
WAGR syndrome.
Shimamura Y, Okamoto T, Abe K, Takuto M, Ogawa Y, Takizawa H. Shimamura Y, et al. Kidney Int. 2021 Jan;99(1):271. doi: 10.1016/j.kint.2020.05.017. Kidney Int. 2021. PMID: 33390234 Free article. No abstract available.
WAGR syndrome: a clinical review of 54 cases.
Fischbach BV, Trout KL, Lewis J, Luis CA, Sika M. Fischbach BV, et al. Pediatrics. 2005 Oct;116(4):984-8. doi: 10.1542/peds.2004-0467. Pediatrics. 2005. PMID: 16199712 Review.
Although the genotypic defects in WAGR syndrome have been well established, the large variety of phenotypic manifestations of the syndrome has never been reported. ...Recommendations for diagnosis, evaluation, and surveillance of patients with WAGR …
Although the genotypic defects in WAGR syndrome have been well established, the large variety of phenotypic manifestations of …
WT1-related disorders: more than Denys-Drash syndrome.
Lopez-Gonzalez M, Ariceta G. Lopez-Gonzalez M, et al. Pediatr Nephrol. 2024 Sep;39(9):2601-2609. doi: 10.1007/s00467-024-06302-y. Epub 2024 Feb 7. Pediatr Nephrol. 2024. PMID: 38326647 Review.
Historically, specific mutations in WT1 gene have been associated with distinct syndromes based on phenotypic characteristics, including Denys-Drash syndrome (DDS), Frasier syndrome (FS), Meacham syndrome, and WAGR syndrome. DDS is classically d …
Historically, specific mutations in WT1 gene have been associated with distinct syndromes based on phenotypic characteristics, including Den …
Visual Acuity in Aniridia and WAGR Syndrome.
Krause MA, Trout KL, Lauderdale JD, Netland PA. Krause MA, et al. Clin Ophthalmol. 2023 May 1;17:1255-1261. doi: 10.2147/OPTH.S405003. eCollection 2023. Clin Ophthalmol. 2023. PMID: 37152637 Free PMC article.
Aniridia subjects were age- and gender-matched with WAGR syndrome subjects in the Coordination of Rare Diseases at Sanford (CoRDS) database. ...Our results suggest that visual acuity may indicate severity of ocular involvement and variability of phenotype in aniridi …
Aniridia subjects were age- and gender-matched with WAGR syndrome subjects in the Coordination of Rare Diseases at Sanford (Co …
[WAGR syndrome].
Kaneko Y. Kaneko Y. Nihon Rinsho. 2006 Sep 28;Suppl 3:605-8. Nihon Rinsho. 2006. PMID: 17022619 Review. Japanese. No abstract available.
Sleep problems in youth with WAGR syndrome.
Kalish-Schur GB, Somayaji M, Meltzer LJ, Cielo CM. Kalish-Schur GB, et al. Sleep Med. 2025 Feb 17;129:101-104. doi: 10.1016/j.sleep.2025.02.018. Online ahead of print. Sleep Med. 2025. PMID: 40015216

Melatonin was used for sleep in 7 (47 %) youth with WAGR syndrome versus 3 (11 %) controls (p = 0.009). PSQ-SRBD scores were greater in youth with WAGR syndrome (0.52 [0.45, 0.65]) compared to controls (0.09 [0.05, 0.18], p < 0.001); 93 % of youth w

…
Melatonin was used for sleep in 7 (47 %) youth with WAGR syndrome versus 3 (11 %) controls (p = 0.009). PSQ-SRBD scores were g …
Results From the WAGR Syndrome Patient Registry: Characterization of WAGR Spectrum and Recommendations for Care Management.
Duffy KA, Trout KL, Gunckle JM, Krantz SM, Morris J, Kalish JM. Duffy KA, et al. Front Pediatr. 2021 Dec 14;9:733018. doi: 10.3389/fped.2021.733018. eCollection 2021. Front Pediatr. 2021. PMID: 34970513 Free PMC article.
WAGR syndrome is a rare genetic disorder characterized by Wilms tumor, Aniridia, Genitourinary anomalies, and Range of developmental delays. ...This suggests that a broader phenotypic spectrum beyond the classic syndrome exists and here we demonstrate that sp …
WAGR syndrome is a rare genetic disorder characterized by Wilms tumor, Aniridia, Genitourinary anomalies, and Range of develop …
PAX6-Related Aniridia.
Moosajee M, Hingorani M, Moore AT. Moosajee M, et al. 2003 May 20 [updated 2018 Oct 18]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2003 May 20 [updated 2018 Oct 18]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 20301534 Free Books & Documents. Review.
Because of the increased risk for renal impairment in WAGR syndrome (especially in those with bilateral Wilms tumor), lifelong evaluation of renal function is recommended. ...GENETIC COUNSELING: Isolated aniridia and WAGR syndrome are inherited in an a …
Because of the increased risk for renal impairment in WAGR syndrome (especially in those with bilateral Wilms tumor), lifelong …
Prenatal Diagnosis of WAGR Syndrome.
Tezcan B, Rich P, Bhide A. Tezcan B, et al. Case Rep Obstet Gynecol. 2015;2015:928585. doi: 10.1155/2015/928585. Epub 2015 Oct 28. Case Rep Obstet Gynecol. 2015. PMID: 26605098 Free PMC article.
Wilm's tumour, aniridia, genitourinary abnormalities, and mental retardation (WAGR) syndrome is a rare genetic disorder with an estimated prevalence of 1 in 500,000 to 1 million. ...Children with WAGR syndrome mostly present in the newborn/infancy peri …
Wilm's tumour, aniridia, genitourinary abnormalities, and mental retardation (WAGR) syndrome is a rare genetic disorder with a …
272 results