Literature DB >> 23933668

Primary hypothyroidism: an unusual manifestation of Wolcott-Rallison syndrome.

Betül Ersoy1, Bayram Özhan, Seniha Kiremitçi, Oscar Rubio-Cabezas, Sian Ellard.   

Abstract

Wolcott-Rallison syndrome has been reported to be associated with early-onset diabetes, epiphyseal dysplasia, hepatic and renal dysfunction, mental retardation, severe growth retardation, neutropenia, exocrine pancreatic dysfunction, and central hypothyroidism. We report on primary hypothyroidism, which has not been previously described, of a patient with Wolcott-Rallison syndrome due to novel mutation (W521X), who showed improved growth after thyroid hormone treatment.

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Year:  2013        PMID: 23933668     DOI: 10.1007/s00431-013-2110-8

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  10 in total

1.  Wolcott-Rallison syndrome: a case with endocrine and exocrine pancreatic deficiency and pancreatic hypotrophy.

Authors:  P Castelnau; M Le Merrer; C Diatloff-Zito; E Marquis; M J Tête; J J Robert
Journal:  Eur J Pediatr       Date:  2000-08       Impact factor: 3.183

2.  Endoplasmic reticulum stress decreases intracellular thyroid hormone activation via an eIF2a-mediated decrease in type 2 deiodinase synthesis.

Authors:  Rafael Arrojo E Drigo; Tatiana L Fonseca; Melany Castillo; Matthias Salathe; Gordana Simovic; Petra Mohácsik; Balazs Gereben; Antonio C Bianco
Journal:  Mol Endocrinol       Date:  2011-11-03

Review 3.  Wolcott-Rallison syndrome due to the same mutation (W522X) in EIF2AK3 in two unrelated families and review of the literature.

Authors:  M Nuri Ozbek; Valérie Senée; Sehnaz Aydemir; L Damla Kotan; Neslihan O Mungan; Bilgin Yuksel; Cécile Julier; A Kemal Topaloglu
Journal:  Pediatr Diabetes       Date:  2010-02-25       Impact factor: 4.866

4.  Perk is essential for translational regulation and cell survival during the unfolded protein response.

Authors:  H P Harding; Y Zhang; A Bertolotti; H Zeng; D Ron
Journal:  Mol Cell       Date:  2000-05       Impact factor: 17.970

Review 5.  Assessment of iodine nutrition in populations: past, present, and future.

Authors:  Michael B Zimmermann; Maria Andersson
Journal:  Nutr Rev       Date:  2012-10       Impact factor: 7.110

Review 6.  Wolcott-Rallison syndrome: a clinical and genetic study of three children, novel mutation in EIF2AK3 and a review of the literature.

Authors:  S Iyer; M Korada; L Rainbow; J Kirk; R M Brown; N Shaw; T G Barrett
Journal:  Acta Paediatr       Date:  2004-09       Impact factor: 2.299

7.  Wolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous families.

Authors:  Oscar Rubio-Cabezas; Ann-Marie Patch; Jayne A L Minton; Sarah E Flanagan; Emma L Edghill; Khalid Hussain; Amina Balafrej; Asma Deeb; Charles R Buchanan; Ian G Jefferson; Angham Mutair; Andrew T Hattersley; Sian Ellard
Journal:  J Clin Endocrinol Metab       Date:  2009-10-16       Impact factor: 5.958

8.  Endoplasmic reticulum stress induces hepatic steatosis via increased expression of the hepatic very low-density lipoprotein receptor.

Authors:  Hyunsun Jo; Sung Sik Choe; Kyung Cheul Shin; Hagoon Jang; Jae Ho Lee; Je Kyung Seong; Sung Hoon Back; Jae Bum Kim
Journal:  Hepatology       Date:  2013-04       Impact factor: 17.425

9.  Wolcott-Rallison syndrome: diabetes mellitus and spondyloepiphyseal dysplasia.

Authors:  H Stöss; H J Pesch; B Pontz; A Otten; J Spranger
Journal:  Eur J Pediatr       Date:  1982-03       Impact factor: 3.183

10.  Wolcott-Rallison syndrome in two siblings with isolated central hypothyroidism.

Authors:  Bassam Bin-Abbas; Abdulmohsen Al-Mulhim; Abdullah Al-Ashwal
Journal:  Am J Med Genet       Date:  2002-08-01
  10 in total
  2 in total

1.  Liver disease and other comorbidities in Wolcott-Rallison syndrome: different phenotype and variable associations in a large cohort.

Authors:  Abdelhadi M Habeb; Asma Deeb; Matthew Johnson; Mohammed Abdullah; Majidah Abdulrasoul; Hussain Al-Awneh; Mohammed S F Al-Maghamsi; Fathiya Al-Murshedi; Ramlah Al-Saif; Siham Al-Sinani; Dina Ramadan; Hala Tfayli; Sarah E Flanagan; Sian Ellard
Journal:  Horm Res Paediatr       Date:  2015-02-05       Impact factor: 2.852

2.  EIF2AK3 novel mutation in a child with early-onset diabetes mellitus, a case report.

Authors:  Tarah H Fatani
Journal:  BMC Pediatr       Date:  2019-03-28       Impact factor: 2.125

  2 in total

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