A case of Hoyeraal-Hreidarsson syndrome: Delayed myelination and hypoplasia of corpus callosum are other important signs

被引:16
作者
Akaboshi, S
Yoshimura, M
Hara, T
Kageyama, H
Nishikwa, K
Kawakami, T
Ieshima, A
Takeshita, K
机构
[1] Tottori Univ, Fac Med, Inst Neurol Sci, Div Child Neurol, Yonago, Tottori 6838504, Japan
[2] Tottori Univ, Fac Med, Dept Pediat, Yonago, Tottori 6838504, Japan
[3] Tottori Prefectural Kaike Rehabil Ctr Disabled Ch, Dept Pediat, Yonago, Tottori, Japan
关键词
cerebellar ataxia; delayed myelination; pancytopenia; thrombocytopenia; immunodeficiency; Hoyeraal-Hreidarsson syndrome;
D O I
10.1055/s-2000-7531
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We report the case of a 7-year old girl with Hayeraal-Hreidarsson syndrome (HHS) and review other cases of HHS. In addition to the previously described important signs of HHS, i.e., prenatal growth retardation, microcephaly, psychomotor retardation, progressive pancytopenia, immunological abnormalities, and cerebellar hypoplasia and ataxia, we consider that delayed myelination of cerebral white matter and hypoplastic corpus callosum should be added to the list of important signs. However, it is not clear whether delayed myelination of white matter in HHS indicates dysmyelination or demyelination, Furthermore, we suggest that immunological abnormalities of both T and B cells are one of the important signs of HHS. We consider these new important signs to be valuable for the diagnosis of HHS.
引用
收藏
页码:141 / 144
页数:4
相关论文
共 15 条
  • [1] AALFS CM, 1995, EUR J PEDIATR, V154, P304, DOI 10.1007/BF01957367
  • [2] THE HOYERAAL-HREIDARSSON SYNDROME - DONT FORGET THE ASSOCIATED IMMUNODEFICIENCY
    BERTHET, F
    TUCHSCHMID, P
    BOLTSHAUSER, E
    SEGER, RA
    [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1995, 154 (12) : 998 - 998
  • [3] BERTHET F, 1994, EUR J PEDIATR, V153, P333
  • [4] RELATIVE INCREASE OF T-CELLS EXPRESSING THE GAMMA-DELTA RATHER THAN THE ALPHA-BETA RECEPTOR IN ATAXIA TELANGIECTASIA
    CARBONARI, M
    CHERCHI, M
    PAGANELLI, R
    GIANNINI, G
    GALLI, E
    GAETANO, C
    PAPETTI, C
    FIORILLI, M
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1990, 322 (02) : 73 - 76
  • [5] GIAMPIETRO PF, 1993, PEDIATRICS, V91, P1116
  • [6] CHEMICAL MUTAGEN HYPERSENSITIVITY IN ATAXIA TELANGIECTASIA
    HOAR, DI
    SARGENT, P
    [J]. NATURE, 1976, 261 (5561) : 590 - 592
  • [7] CONGENITAL HYPOPLASTIC THROMBOCYTOPENIA AND CEREBRAL MALFORMATIONS IN 2 BROTHERS
    HOYERAAL, HM
    LAMVIK, J
    [J]. ACTA PAEDIATRICA SCANDINAVICA, 1970, 59 (02): : 185 - &
  • [8] A SYNDROME OF PROGRESSIVE PANCYTOPENIA WITH MICROCEPHALY, CEREBELLAR HYPOPLASIA AND GROWTH FAILURE
    HREIDARSSON, S
    KRISTJANSSON, K
    JOHANNESSON, G
    JOHANNSSON, JH
    [J]. ACTA PAEDIATRICA SCANDINAVICA, 1988, 77 (05): : 773 - 775
  • [9] ATAXIA-PANCYTOPENIA - SYNDROME OF CEREBELLAR-ATAXIA, HYPOPLASTIC-ANEMIA, MONOSOMY-7, AND ACUTE MYELOGENOUS LEUKEMIA
    LI, FP
    HECHT, F
    KAISERMCCAW, B
    BARANKO, PV
    POTTER, NU
    [J]. CANCER GENETICS AND CYTOGENETICS, 1981, 4 (03) : 189 - 196
  • [10] Familial cerebellar hypoplasia and pancytopenia without chromosomal breakages
    Mahmood, F
    King, MD
    Smyth, OP
    Farrell, MA
    [J]. NEUROPEDIATRICS, 1998, 29 (06) : 302 - 306