Wolfram syndrome. Report of 3 cases;Le syndrome de Wolfram. A propos de 3 cas

Progres en Urologie

Volumn 11, Issue 6, 2001, Pages 1292-1297

  Benchekroun, Abdellatif ^a   Nouini, Yassine ^a,b   Iken, Ali ^a   Iraqui, Mohamed ^a   El Alj, Haj Ahmed ^a   Ould Jdoud, Cheikhani ^a  

^a AVICENNE HOSPITAL   (France)

^b NONE   (Morocco)

Author keywords

DIDMOAD; Urinary manifestations; Wolfram

Indexed keywords

ADOLESCENT; CASE REPORT; CHILD; FEMALE; HUMAN; MALE; REVIEW; WOLFRAM SYNDROME;

ADOLESCENT; CHILD; FEMALE; HUMANS; MALE; WOLFRAM SYNDROME;

EID: 0035752283     PISSN: 11667087     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (29)

1. ABOSEIF S., GASPARINI M., SCHMIDT R., TANAGO E. Wolfram's (DIDMOAD) syndrome and its urological manifestations. Br. J. Urol., 1993, 72 :106-111.
2. ANKOTCHE A., DELMAS V., LARGER E. Insuffisance rénale aiguë chez un patient diabétique. Diabete Metab., 1998, 3, 256-259.
3. BARRETT T. G. , BUNDEY S. E., McLEOD A. F., Neurodegeneretion and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome. Lancet, 1995, 346: 1458-1463.
4. BARRETT T. G., BUNDEY S. E. Wolfram (DIDMOAD) syndrome. J. Med. Genet., 1997, 10, 838-841. Review.
5. BLASI C., PIERELLI E., RISPOLE E., SAPONARA M., VINGOLO E., ANDREANI D. Wolfram's syndrome : a clinical diagnostic and interpretive contribution. Diabetes care, 1986, 9 : 521-528.
6. CAIONE P., MAZZEO D., DI MARCO A., CAPOZZA N., CERIATI E. Wolfram syndrome. Peculiar urologie aspects. Minerva Pediatr. , 1995, 47, 77-81
7. CHU P., STAFF W. G., MORRIS J. A., POLLAK J. M. DIDMOAD syndrome with megacystis and megaureter. Postgrad. Med. J. , 1986, 62: 859-863.
8. CREMERS C. W. R. J. , WIJDEVELD P. G. A. B. , PINCKERS A. J. L. G. Juvenile Diabetes mellitus, optic atrophy, hearing loss, diabetes insipidus, atonia of the urinary tract and bladder and over abnormalities (Wolfram syndrome). Acta Paediatr. Scand. , 1977, Suppl., S264: 2-16.
9. DAVID A., COLLIER T.G., BARRETT, DAVID CURTIS, ANDREW MAC LEOD, MARIA J. ARRANZ, J. ANTONIE MAASSEN, BUNDEY S. Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneity Am. J. Hum. Genet., 1996, 59: 855-863.
10. DREYER M., RUDIGER H. W., BUJARA A., HERBERHOLD C., KUHNAU J., MAACK P., BARTHELHEIMER H. The syndrome of diabetes insipidus, diabetes mellitus, optic atrophy, deafness and over abnormalities (DIDMOAD-syndrome). Klin. Wochenschr., 1982, 60: 471-475.
11. EL-SHANTI H., LIDRAL A. C., JARRAH N., DRUHAN L., AJLOUNI K. Homozygosity mapping identifies an additional locus for Wolfram syndrome on chromosome 4q. Am. J. Hum. Genet., 2000, 66, 1229-1236.
12. FRANÇOIS P., N'G VAN NHAN, LEVY G., GRATALOUP G., FAURE G., M. BOST. Les manifestations urinaires du syndrome de Wolfram. Pédiatrie, 1982, 37, 119-124.
13. FRASER G.R. Heredity in juvenile diabetes. Br. Med. J., 1964, 1, 433-434.
14. GALLUZZI P., FILOSOMI G., VALLONE I. M., BARDELLI A.M., VENTURI C. MRI of Wolfram syndrome (DIDMOAD). Neuroradiology, 1999, 41, 729-731.
15. GUNN T., BORTOLUSSI R., LITTLE J., ANDERMANN F. , CLARKE F. C. , BELMONTE M. Juvenile diabetes mellitus, optic atrophy, sensory nerve deafness, and diabetes insipidus: a syndrome. J. Pediatr. , 1976, 89 :565-570.
16. HAFTEL L. T., LEV D., BARASH V. GUTMAN A., BUJANOVER Y. LERMAN-SAGIE T. Familial mitochondrial intestinal pseudo-obstruction and neurogenic bladder. J. Child Neurol., 2000, 15, 386-389.
17. KINSLEY B.T., SWIFT M., DUMONT R.H., SWIFT R. G. Morbidity and mortality in the Wolfram syndrome. Diabetes Care, 1995, 18, 1566-1570.
18. MARQUARDT J. L , LORIAUX L. Diabetes mellitus and optic atrophy. Arch. Int. Med. , 1974, 134, 32-37.
19. MIDDLE F., JONES I., McCANDLESS F., BARRETT T., KHANIM F., OWEN M.J., LENDON C., CRADDOCK N. Bipolar disorder and variation at a common polymorphism (A1832G) within exon 8 of the Wolfram gene. Am. J. Med. Genet. , 2000, 96, 154-157.
20. MONLLOR GISBERT J., TANO PINO F., RODRIGUEZ ARTEAGA P., GALBIS PALAU F. Urologie manifestations in Wolfram's syndrome. Actas Urol. Esp. , 1996, 20, 474-477.
21. NAGI N. A., Dibetes insipidus, diabetes mellitus, optic atrophy and deafness. A clinical and genetic study. Postgrad. Med. J. , 1979, 55: 377-380.
22. PAGE M. M. C. B., ASMAL A. C., EDWARDS C. R. W. Recessive inheritance of diabetes : the syndrome of diabetes insipidus. diabetes mellitus, optic atrophy and deafness. Q. J. Med., 1976, 179 : 505-520.
23. PEDEN N. R., GAY J. D. L., JUNG L. T., KUWAYTI K. Wolfram (DIDMOAD) syndrome : a complex long term problem in management. Q. J. Med., 1986, 58 : 167-180.
24. POLYMOUROPOULOS M., SWIFT R., SWIFT M., Linkage of the gene for Wolfram syndrome to markers on the short arm of the chromosome 4. Nature Genet., 1994, 8 : 95-97.
25. SCOLDING N.J., KELLAR-WOOD H.F., SCHAW C., SHNEERSON J.M., ANTOUN N. Wolfram syndrome: hereditary diabetes mellitus with brainstem and optic atrophy. Ann. Neurol, 1996, 39 : 352-360.
26. SHAW D. A., DUNCAN L. J. P. Optic atrophy and nerve deafness in diabetes mellitus. J. Neurol. Neurosurg. Psychiatry, 1958, 21 : 47-49.
27. STROM T. M., HORTNAGEL K , HOFMANN S., GEKELER F., SCHARFE C., RABL W., GERBITZ K.D., MEITINGER T. Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein. Hum. Mol. Genet., 1998, 7, 2021-2028.
28. TEKGUL S., OGE O., SIMSEK E., YORDAM N., KENDI S. : Urological manifestations of the Wolfram syndrome: observations in 14 patients. J. Urol., 1999, 161, 616-617.
29. WOLFRAM D.J.: Diabetes mellitus and simple optic atrophy among siblings: report of four cases. Proc. Mayo. Clin., 1938, 13: 715-718.