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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.
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
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 …
Wolcott-Rallison syndrome due to the same mutation (W522X) in EIF2AK3 in two unrelated families and review of the literature.
Ozbek MN, Senée V, Aydemir S, Kotan LD, Mungan NO, Yuksel B, Julier C, Topaloglu AK. Ozbek MN, et al. Pediatr Diabetes. 2010 Jun;11(4):279-85. doi: 10.1111/j.1399-5448.2009.00591.x. Epub 2010 Feb 25. Pediatr Diabetes. 2010. PMID: 20202148 Review.
Wolcott-Rallison syndrome (WRS) is a rare autosomal recessive disorder characterized by an early-infancy-onset diabetes mellitus associated with a variety of multisystemic clinical manifestations. ...Other than the consistent features of diabetes mellitus and epiphy
Wolcott-Rallison syndrome (WRS) is a rare autosomal recessive disorder characterized by an early-infancy-onset diabetes mellit
Liver, pancreas and kidney transplantation for the treatment of Wolcott-Rallison syndrome.
Tzakis AG, Nunnelley MJ, Tekin A, Buccini LD, Garcia J, Uchida K, Neville HL, Nares MA, Ruiz P, Bodamer O. Tzakis AG, et al. Am J Transplant. 2015 Feb;15(2):565-7. doi: 10.1111/ajt.13005. Epub 2014 Nov 10. Am J Transplant. 2015. PMID: 25384546 Free article. Review.
We present the case of a child who underwent a combined liver, pancreas and double kidney transplant following complications of Wolcott-Rallison syndrome (WRS) a rare genetic disorder that causes infantile insulin-dependent diabetes mellitus (IDDM) and often death i …
We present the case of a child who underwent a combined liver, pancreas and double kidney transplant following complications of Wolcott