Literature DB >> 17297000

Wolfram syndrome presenting marked brain MR imaging abnormalities with few neurologic abnormalities.

S Ito1, R Sakakibara, T Hattori.   

Abstract

Wolfram syndrome is a rare autosomal recessive disorder featuring diabetes insipidus, diabetes mellitus, optic atrophy, and deafness; DIDMOAD is a commonly accepted anonym for this disorder. We describe a 35-year-old man with Wolfram syndrome, who had marked atrophy of the brain stem, middle cerebellar peduncle, and cerebellum. Despite these MR imaging findings involving the pontocerebellar tract, the patient had no neurologic abnormalities suggesting dysfunction of the brain stem or cerebellum. Patients with Wolfram syndrome may have discrepancies between neurologic and radiologic findings.

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Year:  2007        PMID: 17297000      PMCID: PMC7977398     

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  14 in total

1.  Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.

Authors:  K Bürk; M Abele; M Fetter; J Dichgans; M Skalej; F Laccone; O Didierjean; A Brice; T Klockgether
Journal:  Brain       Date:  1996-10       Impact factor: 13.501

2.  Supratentorial atrophy in spinocerebellar ataxia type 2: MRI study of 20 patients.

Authors:  S Giuffrida; R Saponara; D A Restivo; A Trovato Salinaro; L Tomarchio; P Pugliares; G Fabbri; C Maccagnano
Journal:  J Neurol       Date:  1999-05       Impact factor: 4.849

3.  Spinocerebellar ataxia type 1 with multiple system degeneration and glial cytoplasmic inclusions.

Authors:  S Gilman; A A Sima; L Junck; K J Kluin; R A Koeppe; M E Lohman; R Little
Journal:  Ann Neurol       Date:  1996-02       Impact factor: 10.422

4.  Atrophy of the cerebellum and brainstem in dentatorubral pallidoluysian atrophy. Influence of CAG repeat size on MRI findings.

Authors:  R Koide; O Onodera; T Ikeuchi; R Kondo; H Tanaka; S Tokiguchi; A Tomoda; T Miike; F Isa; H Beppu; N Shimizu; Y Watanabe; Y Horikawa; T Shimohata; K Hirota; A Ishikawa; S Tsuji
Journal:  Neurology       Date:  1997-12       Impact factor: 9.910

5.  Wolfram syndrome: a neuropathological study.

Authors:  D Genís; A Dávalos; A Molins; I Ferrer
Journal:  Acta Neuropathol       Date:  1997-04       Impact factor: 17.088

6.  Radiological findings in Wolfram syndrome.

Authors:  Azmy M Hadidy; Nadim S Jarrah; Maha I Al-Till; Hatem E El-Shanti; Kamel M Ajlouni
Journal:  Saudi Med J       Date:  2004-05       Impact factor: 1.484

7.  Dentatorubral-pallidoluysian atrophy (DRPLA): clinical, genetic, and neuroradiologic studies in a family.

Authors:  E Uyama; I Kondo; M Uchino; T Fukushima; N Murayama; A Kuwano; N Inokuchi; Y Ohtani; M Ando
Journal:  J Neurol Sci       Date:  1995-06       Impact factor: 3.181

8.  Wolfram syndrome: hereditary diabetes mellitus with brainstem and optic atrophy.

Authors:  N J Scolding; H F Kellar-Wood; C Shaw; J M Shneerson; N Antoun
Journal:  Ann Neurol       Date:  1996-03       Impact factor: 10.422

9.  Psychiatric findings in Wolfram syndrome homozygotes.

Authors:  R G Swift; D B Sadler; M Swift
Journal:  Lancet       Date:  1990-09-15       Impact factor: 79.321

10.  Wolfram (DIDMOAD) syndrome: a multidisciplinary clinical study in nine Turkish patients and review of the literature.

Authors:  E Simsek; T Simsek; S Tekgül; S Hosal; V Seyrantepe; G Aktan
Journal:  Acta Paediatr       Date:  2003       Impact factor: 2.299

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  13 in total

1.  Balance impairment in individuals with Wolfram syndrome.

Authors:  Kristen A Pickett; Ryan P Duncan; Alex R Paciorkowski; M Alan Permutt; Bess Marshall; Tamara Hershey; Gammon M Earhart
Journal:  Gait Posture       Date:  2012-07-06       Impact factor: 2.840

2.  Wolfram syndrome: clinical and genetic profiling of a cohort from a tertiary care centre with characterization of the primary gonadal failure.

Authors:  Liza Das; Ashutosh Rai; Ravimohan Mavuduru; Kim Vaiphei; Akhilesh Sharma; Vishali Gupta; Sanjay Kumar Bhadada; Sailesh Lodha; Naresh Panda; Anil Bhansali; Paramjeet Singh; Pinaki Dutta
Journal:  Endocrine       Date:  2020-04-29       Impact factor: 3.633

Review 3.  WS1 gene mutation analysis of Wolfram syndrome in a Chinese patient and a systematic review of literatures.

Authors:  Guang Yu; Man-li Yu; Jia-feng Wang; Cong-rong Gao; Zhong-jin Chen
Journal:  Endocrine       Date:  2010-10-23       Impact factor: 3.633

Review 4.  Endocrine and metabolic aspects of the Wolfram syndrome.

Authors:  Georgios Boutzios; Sarantis Livadas; Evangelos Marinakis; Nicole Opie; Frangiskos Economou; Evanthia Diamanti-Kandarakis
Journal:  Endocrine       Date:  2011-08       Impact factor: 3.633

5.  Wolfram Syndrome: A rare cause of progressive cerebellar ataxia.

Authors:  Fernanda Subtil de Moraes Machado; André Eduardo de Almeida Franzoi; Goretti Silveira Rodrigues; Rafael Silva Menegatti; Claudio Rogerio Werka Junior; Paulo Roberto Wille; Audred Cristina Biondo Eboni; Marcus Vinícius Magno Gonçalves
Journal:  Neurol Clin Pract       Date:  2019-12

6.  Longitudinal Assessment of Neuroradiologic Features in Wolfram Syndrome.

Authors:  A Samara; H M Lugar; T Hershey; J S Shimony
Journal:  AJNR Am J Neuroradiol       Date:  2020-10-29       Impact factor: 3.825

Review 7.  Genetic and clinical aspects of Wolfram syndrome 1, a severe neurodegenerative disease.

Authors:  Luciana Rigoli; Placido Bramanti; Chiara Di Bella; Filippo De Luca
Journal:  Pediatr Res       Date:  2018-02-28       Impact factor: 3.756

Review 8.  Clinical Spectrum Associated with Wolfram Syndrome Type 1 and Type 2: A Review on Genotype-Phenotype Correlations.

Authors:  Maurizio Delvecchio; Matteo Iacoviello; Antonino Pantaleo; Nicoletta Resta
Journal:  Int J Environ Res Public Health       Date:  2021-04-30       Impact factor: 3.390

9.  Central nervous system PET-CT imaging reveals regional impairments in pediatric patients with Wolfram syndrome.

Authors:  Agnieszka Zmyslowska; Bogdan Malkowski; Wojciech Fendler; Maciej Borowiec; Karolina Antosik; Piotr Gnys; Dobromila Baranska; Wojciech Mlynarski
Journal:  PLoS One       Date:  2014-12-26       Impact factor: 3.240

10.  Clinical utility gene card for: Wolfram syndrome.

Authors:  Mariya Moosajee; Patrick Yu-Wai-Man; Cécile Rouzier; Maria Bitner-Glindzicz; Richard Bowman
Journal:  Eur J Hum Genet       Date:  2016-05-25       Impact factor: 4.246

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