Exercise Intolerance, Malnutrition, Abnormal Sweat Chloride Levels, and Two CFTR Mutations: Is It Cystic Fibrosis?

被引:2
|
作者
Com, Gulnur [1 ]
Uc, Aliye [2 ]
机构
[1] Univ Arkansas Med Sci, Dept Pediat, Pediat Pulmonol, Little Rock, AR 72202 USA
[2] Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA
关键词
Cystic fibrosis; adrenal insufficiency; sweat chloride test; FECAL ELASTASE-1; MARKER;
D O I
10.1016/j.pedhc.2014.05.010
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
[No abstract available]
引用
收藏
页码:201 / 204
页数:4
相关论文
共 50 条
  • [1] Sweat chloride and immunoreactive trypsinogen in infants carrying two CFTR mutations and not affected by cystic fibrosis
    Castellani, Carlo
    Tridello, Gloria
    Tamanini, Anna
    Assael, Baroukh M.
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 2017, 102 (07) : 644 - 646
  • [2] Sweat chloride concentrations and CFTR gene mutations in late diagnosed cystic fibrosis
    Bradley, D. T.
    Beattie, D.
    Graham, C. A.
    Magee, A. C.
    Mckee, S. A.
    Patterson, C. C.
    Rendall, J.
    Elborn, J. S.
    [J]. THORAX, 2007, 62 : A104 - A105
  • [3] Mutations of the cystic fibrosis gene and intermediate sweat chloride levels in children
    Lebecque, P
    Leal, T
    De Boeck, C
    Jaspers, M
    Cuppens, H
    Cassiman, JJ
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 165 (06) : 757 - 761
  • [4] Mutations of CFTR gene and intermediate sweat chloride levels
    Lebecque, P
    De Boeck, K
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2003, 167 (11) : 1577 - 1578
  • [5] GENES OTHER THAN CFTR AFFECT SWEAT CHLORIDE IN CYSTIC FIBROSIS
    Blackman, S. M.
    Collaco, J. M.
    Cutting, G. R.
    [J]. PEDIATRIC PULMONOLOGY, 2012, 47 : 277 - 277
  • [6] Exercise intolerance in cystic fibrosis-the role of CFTR modulator therapies
    Caterini, Jessica E.
    Ratjen, Felix
    Barker, Alan R.
    Williams, Craig A.
    Rendall, Kate
    Schneiderman, Jane E.
    Wells, Greg D.
    [J]. JOURNAL OF CYSTIC FIBROSIS, 2022, 21 (02) : 282 - 292
  • [7] Cystic fibrosis mutations in heterozygous newborns with hypertrypsinemia and low sweat chloride
    Castellani, C
    Benetazzo, MG
    Bonizzato, A
    Pignatti, PF
    Mastella, G
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (01) : 303 - 304
  • [8] Heterogeneity of CFTR modulator-induced sweat chloride concentrations in people with cystic fibrosis
    Zemanick, E. T.
    Emerman, I.
    Mccreary, M.
    Mayer-Hamblett, N.
    Warden, M. N.
    Odem-Davis, K.
    Vandevanter, D. R.
    Ren, C. L.
    Young, J.
    Konstan, M. W.
    [J]. JOURNAL OF CYSTIC FIBROSIS, 2024, 23 (04) : 676 - 684
  • [9] Negative sweat test in hypertrypsinaemic infants with cystic fibrosis carrying rare CFTR mutations
    Padoan, R
    Bassotti, A
    Seia, M
    Corbetta, C
    [J]. EUROPEAN JOURNAL OF PEDIATRICS, 2002, 161 (04) : 212 - 215
  • [10] Negative sweat test in hypertrypsinaemic infants with cystic fibrosis carrying rare CFTR mutations
    Rita Padoan
    Alessandra Bassotti
    Manuela Seia
    Carlo Corbetta
    [J]. European Journal of Pediatrics, 2002, 161 : 212 - 215