Wolfram syndrome: A neuropathological study

被引:43
作者
Genis, D
Davalos, A
Molins, A
Ferrer, I
机构
[1] UNIV BARCELONA,UNIT NEUROPATHOL,SERV PATHOL,PRINCEPS ESPANYA HOSP,E-08907 LHOSPITALET LLOBR,SPAIN
[2] JOSEP TRUETA HOSP,NEUROL UNIT,GIRONA,SPAIN
关键词
Wolfram syndrome; diabetes insipidus; diabetes mellitus; optic atrophy and deafness (DIDMOAD) syndrome;
D O I
10.1007/s004010050635
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Neuropathological examination was carried out on a patient aged 37 years who had suffered from Wolfram syndrome. Atrophy of the olfactory bulbs and tracts, atrophy of the optic nerves and chiasm, loss of neurons in the lateral geniculate nuclei mainly affecting the small cell layers, atrophy of the superior colliculus, loss of fibers in the cochlear nerve and mild loss of neurons in the cochlear nuclei and inferior colliculus, mild olivopontocerebellar atrophy, and demyelination of the pyramidal tracts were the main neuropathological findings. These correlated with anosmia, loss of vision, loss of hearing, cerebellar symptoms and signs, Babinski sign, and clonus, respectively, clinically observed in this patient. Mild neuron loss and gliosis in the preoptic and paraventricular area of the hypothalamus and mild motor neuron loss in the spinal cord did not reach thresholds of impaired function, although loss of neurons in discrete bulbar nuclei might have accounted for the late episode of food aspiration and suffocation. The relationship between memory loss, personality disturbances, and signs of prefrontal release and mild loss of neurons in the anterior and dorsomedial nuclei of the thalamus remains unclear.
引用
收藏
页码:426 / 429
页数:4
相关论文
共 15 条
  • [1] A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome
    Barrientos, A
    Volpini, V
    Casademont, J
    Genis, D
    Manzanares, JM
    Ferrer, I
    Corral, J
    Cardellach, F
    UrbanoMarquez, A
    Estivill, X
    Nunes, V
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (07) : 1570 - 1576
  • [2] MITOCHONDRIAL ABNORMALITIES IN THE DIDMOAD SYNDROME
    BUNDEY, S
    POULTON, K
    WHITWELL, H
    CURTIS, E
    BROWN, IAR
    FIELDER, AR
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1992, 15 (03) : 315 - 319
  • [3] SIMULTANEOUS OCCURRENCE OF DIABETES-MELLITUS, DIABETES-INSIPIDUS, AND OPTIC ATROPHY IN A BROTHER AND SISTER
    CARSON, MJ
    SLAGER, UT
    STEINBERG, RM
    [J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1977, 131 (12): : 1382 - 1385
  • [4] CREMERS C W R J, 1977, Acta Paediatrica Scandinavica Supplement, P1
  • [5] BIOCHEMICAL AND MOLECULAR STUDIES OF MITOCHONDRIAL-FUNCTION IN DIABETES-INSIPIDUS, DIABETES-MELLITUS, OPTIC ATROPHY, AND DEAFNESS
    JACKSON, MJ
    BINDOFF, LA
    WEVER, K
    WILSON, JN
    INCE, P
    ALBERTI, KGMM
    TURNBULL, DM
    [J]. DIABETES CARE, 1994, 17 (07) : 728 - 733
  • [6] KEHL O, 1982, SCHWEIZ MED WSCHR, V112, P348
  • [7] DIABETES-MELLITUS AND OPTIC ATROPHY IN 2 SIBLINGS - A REPORT ON A NEW ASSOCIATION AND A REVIEW OF THE LITERATURE
    KHARDORI, R
    STEPHENS, JW
    PAGE, OC
    DOW, RS
    [J]. DIABETES CARE, 1983, 6 (01) : 67 - 70
  • [8] LEIVASANTANA C, 1993, REV NEUROL, V149, P26
  • [9] ASSOCIATION OF DIABETES-INSIPIDUS, DIABETES-MELLITUS, OPTIC ATROPHY, AND DEAFNESS - THE WOLFRAM OR DIDMOAD SYNDROME
    NAJJAR, SS
    SAIKALY, MG
    ZAYTOUN, GM
    ABDELNOOR, A
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1985, 60 (09) : 823 - 828
  • [10] LINKAGE OF THE GENE FOR WOLFRAM-SYNDROME TO MARKERS ON THE SHORT ARM OF CHROMOSOME-4
    POLYMEROPOULOS, MH
    SWIFT, RG
    SWIFT, M
    [J]. NATURE GENETICS, 1994, 8 (01) : 95 - 97