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Open Access Case Report

Wolfram Syndrome presenting with optic atrophy and diabetes mellitus: two case reports

Masoud Reza Manaviat, Maryam Rashidi* and Seyed Mohammad Mohammadi

Author Affiliations

Yazd Diabetes Research Center, Shahid Sadoughi University of Medical Science, Jomhouri Boulevard, Yazd, 89179-45556, Iran

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Cases Journal 2009, 2:9355  doi:10.1186/1757-1626-2-9355


The electronic version of this article is the complete one and can be found online at: http://www.casesjournal.com/content/2/1/9355


Received:7 July 2009
Accepted:19 December 2009
Published:19 December 2009

© 2009 Manaviat et al; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Wolfram syndrome is the constellation of juvenile onset diabetes mellitus and optic atrophy, known as DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness).

Patients demonstrate diabetes mellitus followed by optic atrophy in the first decade, diabetes insipidus and sensorineural deafness in the second decade, dilated renal outflow tracts early in the third decade, and multiple neurological abnormalities early in the fourth decade.

This study reports two siblings with late diagnosed wolfram syndrome with diabetes insipidus, diabetes mellitus, optic atrophy, deafness and severe urological abnormalities.

In conclusion, cases having early onset insulin-dependent diabetes mellitus and optic atrophy together need to be evaluated with respect to Wolfram.

Background

For the first time in 1938, wolfram described four siblings with diabetes mellitus and optic atrophy [1]. The main features of wolfram syndrome are diabetes mellitus, diabetes insipidus, sensorineural deafness and optic atrophy [2,3]. It is a progressive neurodegenerative disorder in which patients present with nonautoimmune and non-HLA linked diabetes mellitus associated with optic atrophy in the first decade; diabetes insipidus and sensorineural deafness in the second decade; renal tract abnormalities early in the third decade; and multiple neurological abnormalities, like cerebellar ataxia, myoclonus, and psychiatric illness early in the fourth decade [4]. Wolfram patients usually die from central respiratory failure as a result of brain stem atrophy in their third or fourth decade [4]. The clinical phenotype of wolfram shows similarity with mitochondrial disorders, such as maternally inherited diabetes and deafness, mitochondrial encephalopathy, mitochondrial myopathy, lactic acidosis and stroke-like episodes, or Leber's hereditary optic neuropathy and some studies have concentrated on mitochondrial pathology in Wolfram. Mitochondrial disturbances at the biochemical, morphological, and molecular level have been explained in patients with wolfram, but this has not been a strong finding [5-7].

This study reports two siblings with wolfram and described the course of disease in them to draw the attention of health professionals to think of this syndrome in patients with IDDM and optic atrophy.

Case presentation

Case report 1

First case is an Iranian 20-year old female patient admitted to ophthalmology clinic complaining decreased visual acuity. She has suffered progressive visual deterioration since 8 years ago. On fundoscopic examination, bilateral optic atrophy was recognized, and there was no evidence of diabetic retinopathy. Her visual acuity reduced to 20/80 on both sides. Her visual fields demonstrated generalized constriction. IDDM was diagnosed at the age 6, for which she is receiving insulin with rather poor control of her blood sugar. She has a history of nocturia and high urine output (12 liter per day) for 6 years and after that she has had incontinency and since 2 years ago she has had voiding difficulty and has used self intermittent catheterization four times a day. Renal sonography showed pelvicalyceal dilatation in both kidneys equal to hydronephrose grade IV with dilation in proximal of urethra and bladder enlargement secondary to high urine output. Urethral pressure profile shows atonic bladder. Accordingly wolfram was suspected by ophthalmologist and referred her to an endocrinologist. Diabetes insipidus was diagnosed by dehydration test and after starting Minirin drop, urine output decreased and voiding difficulty improved. There was decreased audible acuity by the age of 16 and audiometry showed bilateral high frequency sensorineural hearing loss.

Renal function, hepatic function, thyroid function and other blood test were normal.

Urea: 30 mg/dL, Creatinine: 1 mg/dL, Creatinine clearance = 85 ml/min, Calcium: 10.7 mg/dL, Phosphorus: 4.8 mg/dL, Sodium: 135 mg/dL, Potassium: 4.6 mg/dL, Alanine transaminase (ALT): 40 IU/L, Aspartate transaminase (AST):40 IU/L, Alkaline Phosphatase: 315 U/L, Total Bilirubin: 0.8 mg/dL, Direct Bilirubin: 0.1 mg/dL, T4: 8.4 ng/dL, T3: 120 ng/dL, TSH: 2.5 mU/L, FT4: 1.1 ng/dL.

There was a family history of similar conditions among her brother and one of her cousins. Also she has a 20-year old brother who is normal.

Case report 2

First case has a 14-year old brother, who acquired IDDM at the same age as his sister, and has had a similar course of disease. He was diagnosed with IDDM at the age of 6 years and has been receiving insulin since then. He has had nocturia, polyuria and voiding difficulty for 3 years and has used self intermittent catheterization too. His visual acuity reduced to 20/120 on both sides. On fundoscopic examination, he has bilateral optic atrophy without diabetic retinopathy (Figure 1, and Figure 2). Renal sonography showed pelvicalyceal dilatation in both kidneys equal to hydronephrose grade III with dilation in proximal of urethra and bladder enlargement. Urethral pressure profile shows atonic bladder. Subsequently wolfram was diagnosed for him and Minirin started. Audiogram was normal. Renal and hepatic function, thyroid function and other blood tests were normal.

thumbnailFigure 1. Photographic image of the patient right eye showing optic atrophy without diabetic retinopathy.

thumbnailFigure 2. Photographic image of the patient left eye showing optic atrophy without diabetic retinopathy.

Discussion

Wolfram is a neurodegenerative disease, which incidence is estimated at one in every 770,000 live births [8]. Early-onset IDDM and optic atrophy are believed to be the initial and basic features of the syndrome [9]. Patients usually demonstrate diabetes mellitus associated by optic atrophy in the first decade, sensorineural deafness and diabetes incipidus in the second decade, dilated renal outflow tracts early in the third decade, and several neurological abnormalities early in the fourth decade [10]. The prevalence, severity and age of onset of the various manifestations of this syndrome are not constant in other studies [11]. In our cases diabetes insipidus, optic atrophy and dilated renal outflow tracts were appeared in second decade.

Patients with wolfram demonstrate progressive ophthalmologic symptoms that usually occur after diabetes mellitus. Besides optic atrophy, constriction of visual fields and decline visual acuity and color vision are the other ophthalmological findings in wolfram syndrome [9,12]; however, diabetic retinopathy is rarely observed [10]. Only five cases with Wolfram have been reported without optic atrophy [10]. In our cases, visual acuity of both eyes was 20/80 and 20/120 respectively. Fundus examination revealed optic atrophy, but no sign of diabetic retinopathy was seen. Also, concentric narrowing was present in the field of vision in both cases.

A wide range of urological abnormalities have been observed in Wolfram, including various degrees of upper urinary tract dilatation and bladder dysfunction. An atonic bladder with a large capacity has been mostly reported. Cremers et al. [13] and Barret et al. [4] reported urological abnormalities in 13 and 58% of their patients, respectively, which was seen in our cases as well.

Sensorineural hearing loss or an abnormal audiogram was observed in 39-62% of patients [4,13]. Audiometry showed bilateral high frequency sensorineural hearing loss in one of our cases, but in second case was not seen.

Wolfram is considered to have an autosomal recessive mode of inheritance. Finding from different studies suggest that wolfram is contributed by alternations in genes located on chromosome 4 or alternatively, in the mitochondrial DNA [10]. Since the initial recognition of the WFS 1 gene by Inoue et al. [14], different research has determined more than 50 distinct mutations of this gene. Accordingly, it is postulated that wolfram is genetically heterogenic [10]. We did not perform genetic analyses in our cases; however, our cases' mother, father, and one sibling underwent systemic and ophthalmological examination. There were no manifestations of wolfram in their examinations, but our cases had a cousin with these symptoms that was died from renal disorder.

Conclusion

In summary, IDDM and optic atrophy are the first and essential features of Wolfram followed by development of deafness, diabetes insipidus and urinary tract abnormalities. Generally cases having IDDM and optic atrophy together need to be evaluated with respect to Wolfram. Cases with Wolfram should be followed all their lives. In these cases, rehabilitation to a normal social life is possible with good follow-up and treatment. The disorder should be kept in mind particularly in our part of the world, where consanguinity is prevalent.

Consent

Written informed consent was obtained from the patients for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

MRM carried out ophthalmologic examination and revised the manuscript. MR helped with data collection and drafted the manuscript. SMM participated in the management of the patients. All authors read and approved the final manuscript.

Acknowledgements

This study was supported by Yazd diabetes Research Center of Shahid Sadoughi University of Medical Sciences.

References

  1. Wolfram DJ, Wagener HP: Diabetes mellitus and simple optic atrophy among siblings: report of four cases.

    1938, 715-718.

  2. Barrett TG, Scott-Brown M, Seller A, Bednarz Amy, Poulton K, Poulton J: The mitochondrial genome in Wolfram syndrome.

    J Med Genet 2000, 37(6):463-466. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  3. Kinsley BT, Swift M, Dumont RH, Swift RG: Morbidity and mortality in the Wolfram syndrome.

    Diabetes Care 1995, 18(12):1566. PubMed Abstract | Publisher Full Text OpenURL

  4. Barrett TG, Bundey SE, Macleod AF: Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome.

    Lancet 1995, 346(8988):1458-1463. PubMed Abstract | Publisher Full Text OpenURL

  5. Bu X, Rotter JI: Wolfram syndrome: a mitochondrial-mediated disorder?

    Lancet 1993, 342(8871):598-600. PubMed Abstract | Publisher Full Text OpenURL

  6. Jackson MJ, Bindoff LA, Weber K, Wilson JN, Ince P, Alberti KG, Turnbull DM: Biochemical and molecular studies of mitochondrial function in diabetes insipidus, diabetes mellitus, optic atrophy, and deafness.

    Diabetes Care 1994, 17(7):728. PubMed Abstract | Publisher Full Text OpenURL

  7. Barrientos A, Casademont J, Saiz A, Cardellach F, Volpini V, Solans A, Tolosa E, Urbano-Marquez A, Estivill X, Nunes V: Autosomal recessive Wolfram syndrome associated with an 8.5-kb mtDNA single deletion.

    Am J Hum Genet 1996, 58(5):963. PubMed Abstract | PubMed Central Full Text OpenURL

  8. Barrett TG, Bundey SE: Wolfram (DIDMOAD) syndrome.

    J Med Genet 1997, 34(10):838-841. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  9. Blasi C, Pierelli F, Rispoli E, Saponara M, Vingolo E, Andreani D: Wolfram's syndrome: a clinical, diagnostic, and interpretative contribution.

    Diabetes Care 1986, 9(5):521. PubMed Abstract | Publisher Full Text OpenURL

  10. Seyhmus A, Ugur K, Ihsan C, Kaan U, Hasan K: Wolfram Syndrome: Case Report and Review of the Literature.

    Compr Ther 2007, 33(1):18-20. PubMed Abstract | Publisher Full Text OpenURL

  11. Shaw DA, Ducan JP: Optic atrophy and nerve deafness in diabetes insipidus.

    J Neurol Neurosurg Psychiatry 1958, 2:47. Publisher Full Text OpenURL

  12. Fishman L, Ehrlich RM: Wolfram syndrome: report of four new cases and a review of literature.

    Diabetes Care 1986, 9(4):405. PubMed Abstract | Publisher Full Text OpenURL

  13. Cremers CW, Wijdeveld PG, Pinckers AJ: Juvenile diabetes mellitus, optic atrophy, hearing loss, diabetes insipidus, atonia of the urinary tract and bladder, and other abnormalities (Wolfram syndrome). A review of 88 cases from the literature with personal observations on 3 new patients.

    Acta Paediatr Scand Suppl 1977, 264:1-16. PubMed Abstract | Publisher Full Text OpenURL

  14. Inoue H, Tanizawa Y, Wasson J, Behn P, Kalidas K, Bernal-Mizrachi E, Mueckler M, Marshall H, Donis-Keller H, Crock P, Rogers D, Mikuni M, Kumashiro H, Higashi K, Sobue G, Oka Y, Permutt MA: A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome).

    Nat Genet 1998, 20:143-148. PubMed Abstract | Publisher Full Text OpenURL