RETROSPECTIVE SURVEY OF UREA CYCLE DISORDERS .2. NEUROLOGICAL OUTCOME IN 49 JAPANESE PATIENTS WITH UREA CYCLE ENZYMOPATHIES

被引:38
|
作者
NAGATA, N
MATSUDA, I
MATSUURA, T
OYANAGI, K
TADA, K
NARISAWA, K
KITAGAWA, T
SAKIYAMA, T
YAMASHITA, F
YOSHINO, M
机构
[1] KUMAMOTO UNIV,SCH MED,DEPT PEDIAT,KUMAMOTO 860,JAPAN
[2] SAPPORO MED COLL,DEPT PEDIAT,SAPPORO,HOKKAIDO 060,JAPAN
[3] TOHOKU UNIV,SCH MED,DEPT PEDIAT,SENDAI,MIYAGI 980,JAPAN
[4] TOHOKU UNIV,SCH MED,DEPT BIOCHEM GENET,SENDAI,MIYAGI 980,JAPAN
[5] NIHON UNIV,SCH MED,DEPT PEDIAT,TOKYO 101,JAPAN
[6] KURUME UNIV,SCH MED,DEPT PEDIAT & CHILD HLTH,KURUME,FUKUOKA 830,JAPAN
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1991年 / 40卷 / 04期
关键词
DQ; IQ; EEG; CT SCAN;
D O I
10.1002/ajmg.1320400421
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We analyzed neurological data, including DQ or IQ, EEG, and CT scan, in 49 patients with urea cycle enzymopathies, all of whom were included in a retrospective survey from 1978-1988 in Japan. We classified 3 groups depending on age-at-onset: group 1 (0-28 days, N = 11), group 2 (29 days-5 years, N = 31), and group 3 (> 5 years, N = 7). The least DQ or IQ score and the highest CT score, representing the most severe brain damage was found in group 1, and the highest DQ or IQ and the least CT score was found in group 3. Intermediate scores of both parameters were found in group 2. There was a negative correlation between these 2 parameters (r = -0.82, P < 0.01). Abnormal EEG during the attack-free period was predominantly observed in patients with CT abnormalities compared to those with a normal CT scan (P < 0.01). Approximately 40% of the patients, mostly in groups 2 and 3 (92.8%) had normal findings in all 3 parameters. Thus, the magnitude of developmental abnormalities is clearly related to the degree of brain damage and to the age-at-onset of these diseases.
引用
收藏
页码:477 / 481
页数:5
相关论文
共 50 条
  • [21] Diagnosis and treatment of urea cycle disorders in adult patients
    Maillot, F.
    Blasco, H.
    Lioger, B.
    Bigot, A.
    Douillard, C.
    REVUE DE MEDECINE INTERNE, 2016, 37 (10): : 680 - 684
  • [22] ANATOMICAL PATHOLOGICAL FINDINGS IN PATIENTS WITH UREA CYCLE DISORDERS
    Yaplito-Lee, J.
    Chow, C. W.
    Boneh, A.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2011, 34 : S89 - S89
  • [23] Histopathological findings in livers of patients with urea cycle disorders
    Yaplito-Lee, Joy
    Chow, Chung-Wo
    Boneh, Avihu
    MOLECULAR GENETICS AND METABOLISM, 2013, 108 (03) : 161 - 165
  • [24] Glutamine and hyperammonemic crises in patients with urea cycle disorders
    Lee, B.
    Diaz, G. A.
    Rhead, W.
    Lichter-Konecki, U.
    Feigenbaum, A.
    Berry, S. A.
    Le Mons, C.
    Bartley, J.
    Longo, N.
    Nagamani, S. C.
    Berquist, W.
    Gallagher, R. C.
    Harding, C. O.
    McCandless, S. E.
    Smith, W.
    Schulze, A.
    Marino, M.
    Rowell, R.
    Coakley, D. F.
    Mokhtarani, M.
    Scharschmidt, B. F.
    MOLECULAR GENETICS AND METABOLISM, 2016, 117 (01) : 27 - 32
  • [25] Long-term outcome of patients with urea cycle disorders and the question of neonatal screening
    Claude Bachmann
    European Journal of Pediatrics, 2003, 162 : S29 - S33
  • [26] Long-term outcome of patients with urea cycle disorders and the question of neonatal screening
    Bachmann, C
    EUROPEAN JOURNAL OF PEDIATRICS, 2003, 162 (Suppl 1) : S29 - S33
  • [27] Understanding biochemical alterations in urea cycle disorders (UCDs) and impact of neurological functioning
    Ellenbogen, Amy
    Ludwig, Wesley
    Shattuck, Kyle
    Gropman, Andrea
    MOLECULAR GENETICS AND METABOLISM, 2012, 105 (03) : 315 - 315
  • [28] LONG-TERM OUTCOME AND INTERVENTION OF UREA CYCLE DISORDERS IN JAPAN
    Endo, F.
    Kido, J.
    Matsumoto, S.
    Mitsubuchi, H.
    Nakamura, K.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2012, 35 : S46 - S46
  • [29] Long-term outcome and intervention of urea cycle disorders in Japan
    Kido, Jun
    Nakamura, Kimitoshi
    Mitsubuchi, Hiroshi
    Ohura, Toshihiro
    Takayanagi, Masaki
    Matsuo, Masafumi
    Yoshino, Makoto
    Shigematsu, Yosuke
    Yorifuji, Tohru
    Kasahara, Mureo
    Horikawa, Reiko
    Endo, Fumio
    JOURNAL OF INHERITED METABOLIC DISEASE, 2012, 35 (05) : 777 - 785
  • [30] Natural history comparison of patients with neonatal proximal versus distal urea cycle disorders: a report from the longitudinal study of urea cycle disorders
    Mew, Nicholas Ah
    Krivitzky, Lauren
    McCarter, Robert
    He, Jianping
    Seminara, Jennifer
    Lee, Hye-Seung
    Tuchman, Mendel
    Batshaw, Mark
    MOLECULAR GENETICS AND METABOLISM, 2012, 105 (03) : 300 - 300