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Quoted phrase not found in phrase index: "Wolcott-Rallison dysplasia"
Page 1
Wolcott-Rallison syndrome.
Juneja A, Sultan A, Bhatnagar S. Juneja A, et al. J Indian Soc Pedod Prev Dent. 2012 Jul-Sep;30(3):250-3. doi: 10.4103/0970-4388.105019. J Indian Soc Pedod Prev Dent. 2012. PMID: 23263430
Multiple epiphyseal dysplasia with early-onset diabetes mellitus (also known as Wolcott-Rallison syndrome) is a rare autosomal recessive disorder that manifests itself in early infancy with symptoms of diabetes mellitus. ...There is usually a short trunk, exc …
Multiple epiphyseal dysplasia with early-onset diabetes mellitus (also known as Wolcott-Rallison syndrome) is a rare au …
Wolcott-Rallison syndrome.
Julier C, Nicolino M. Julier C, et al. Orphanet J Rare Dis. 2010 Nov 4;5:29. doi: 10.1186/1750-1172-5-29. Orphanet J Rare Dis. 2010. PMID: 21050479 Free PMC article. Review.
Wolcott-Rallison syndrome (WRS) is a rare autosomal recessive disease, characterized by neonatal/early-onset non-autoimmune insulin-requiring diabetes associated with skeletal dysplasia and growth retardation. ...WRS should be suspected in any infant who pres …
Wolcott-Rallison syndrome (WRS) is a rare autosomal recessive disease, characterized by neonatal/early-onset non-autoimmune in …
Frequency and spectrum of Wolcott-Rallison syndrome in Saudi Arabia: a systematic review.
Habeb AM. Habeb AM. Libyan J Med. 2013 Jun 10;8(1):21137. doi: 10.3402/ljm.v8i0.21137. Libyan J Med. 2013. PMID: 23759358 Free PMC article. Review.
BACKGROUND: Wolcott-Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neonatal diabetes (PNDM), skeletal dysplasia, and recurrent hepatitis. ...
BACKGROUND: Wolcott-Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neona …
Wolcott-Rallison syndrome: a clinical and genetic study of three children, novel mutation in EIF2AK3 and a review of the literature.
Iyer S, Korada M, Rainbow L, Kirk J, Brown RM, Shaw N, Barrett TG. Iyer S, et al. Acta Paediatr. 2004 Sep;93(9):1195-201. Acta Paediatr. 2004. PMID: 15384883 Review.
BACKGROUND: Wolcott-Rallison syndrome is a rare autosomal recessive condition characterized by early infancy onset diabetes mellitus and multiple epiphyseal dysplasia. ...We have identified a novel 4-base pair deletion (nt 3021-3024 del GAGA) in exon 13, whic …
BACKGROUND: Wolcott-Rallison syndrome is a rare autosomal recessive condition characterized by early infancy onset diabetes me …
Diabetes management in Wolcott-Rallison syndrome: analysis from the German/Austrian DPV database.
Welters A, Meissner T, Konrad K, Freiberg C, Warncke K, Judmaier S, Kordonouri O, Wurm M, Papsch M, Fitzke G, Schmidt SC, Tittel SR, Holl RW. Welters A, et al. Orphanet J Rare Dis. 2020 Apr 22;15(1):100. doi: 10.1186/s13023-020-01359-y. Orphanet J Rare Dis. 2020. PMID: 32321554 Free PMC article.
BACKGROUND: Wolcott-Rallison syndrome (WRS) is characterized by permanent early-onset diabetes, skeletal dysplasia and several additional features, e.g. recurrent liver failure. ...
BACKGROUND: Wolcott-Rallison syndrome (WRS) is characterized by permanent early-onset diabetes, skeletal dysplasia and …
Wolcott-Rallison Syndrome With Different Clinical Presentations and Genetic Patterns in 2 Infants.
Davoodi MA, Karamizadeh Z, Ghobadi F, Shokrpour N. Davoodi MA, et al. Health Care Manag (Frederick). 2018 Oct/Dec;37(4):354-357. doi: 10.1097/HCM.0000000000000238. Health Care Manag (Frederick). 2018. PMID: 30234637
Wolcott-Rallison syndrome is a rare disease presenting with insulin-dependent diabetes mellitus (DM) before 6 months old, skeletal dysplasia after 6 months old, and liver failure. ...Genetic study of patients with insulin-dependent DM before 6 months old, esp …
Wolcott-Rallison syndrome is a rare disease presenting with insulin-dependent diabetes mellitus (DM) before 6 months old, skel …
Wolcott-Rallison syndrome: a case series of three patients.
Memon F, Arif M, Kirmani S, Humayun K. Memon F, et al. Pediatr Endocrinol Diabetes Metab. 2022;28(3):238-240. doi: 10.5114/pedm.2022.118325. Pediatr Endocrinol Diabetes Metab. 2022. PMID: 36106422 Free PMC article.
Walcott-Rallison syndrome has been identified as the most common cause of permanent neonatal diabetes in consanguineous families caused by mutations in eukaryotic translation initiation factor 2-alpha kinase 3 (EIF2AK3), characterized by permanent neonatal diabetes associated wit …
Walcott-Rallison syndrome has been identified as the most common cause of permanent neonatal diabetes in consanguineous families caused by m …
A Genotype-First Approach for Clinical and Genetic Evaluation of Wolcott-Rallison Syndrome in a Large Cohort of Iranian Children With Neonatal Diabetes.
Abbasi F, Habibi M, Enayati S, Bitarafan F, Razzaghy-Azar M, Sotodeh A, Omran SP, Maroofian R, Amoli MM. Abbasi F, et al. Can J Diabetes. 2018 Jun;42(3):272-275. doi: 10.1016/j.jcjd.2017.06.009. Epub 2017 Aug 23. Can J Diabetes. 2018. PMID: 28843469
OBJECTIVE: Wolcott-Rallison syndrome (WRS) is an extremely rare autosomal recessive condition, characterized by permanent neonatal diabetes mellitus (PNDM) associated with skeletal dysplasia, growth retardation and liver dysfunction. ...
OBJECTIVE: Wolcott-Rallison syndrome (WRS) is an extremely rare autosomal recessive condition, characterized by permanent neon …
Relative hypoaldosteronism in a patient with Wolcott-Rallison syndrome.
Uçar A, Aydemir Y, Doğan A, Tunçez E. Uçar A, et al. Diabet Med. 2016 Mar;33(3):e13-6. doi: 10.1111/dme.12968. Diabet Med. 2016. PMID: 26433138
BACKGROUND: Wolcott-Rallison syndrome is an autosomal recessive, multisystem disorder with onset of diabetes in the neonatal period or early infancy. CASE REPORT: A 9-year-old girl with diabetes and growth failure from 2 months of age presented with ketoacidosis and …
BACKGROUND: Wolcott-Rallison syndrome is an autosomal recessive, multisystem disorder with onset of diabetes in the neonatal p …
An Infant With Neonatal Diabetes and Double Outlet Right Ventricle - Wolcott- Rallison syndrome.
Bejiqi R, Retkoceri R, Zeka N, Bejiqi R, Bejic S. Bejiqi R, et al. Med Arch. 2018 Oct;72(4):289-291. doi: 10.5455/medarh.2018.72.289-291. Med Arch. 2018. PMID: 30514997 Free PMC article.
INTRODUCTION: Wolcott-Rallison syndrome (WRS) is a rare, autosomal recessive disorder with infancy-onset diabetes mellitus, multiple epiphyseal dysplasia, osteopenia, mental retardation or developmental delay, and hepatic and renal dysfunction as main clinica …
INTRODUCTION: Wolcott-Rallison syndrome (WRS) is a rare, autosomal recessive disorder with infancy-onset diabetes mellitus, mu …
28 results