Tricho-hepato-enteric syndrome presenting with mild colitis

被引:16
作者
Egritas, Odul [1 ]
Dalgic, Buket [1 ]
Onder, Meltem [2 ]
机构
[1] Gazi Univ, Dept Pediat Gastroenterol, Sch Med, Ankara, Turkey
[2] Gazi Univ, Dept Dermatol, Sch Med, Ankara, Turkey
关键词
Intractable diarrhea; Trichorrhexis nodosa; Tricho-hepato-enteric syndrome; INTRACTABLE DIARRHEA; HEMOCHROMATOSIS; ANOMALIES;
D O I
10.1007/s00431-008-0861-4
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Introduction A four and half-year-old girl was admitted to our clinic with the complaints of diarrhea since birth and failure to thrive. Discussion The characteristic findings in physical examination were facial dysmorphism, hepatomegaly, and wooly hair. Trichorrhexis nodosa was established in microscopic hair examination. Colonoscopy and histopathologic examination of colonic mucosa revealed mild colitis. In the light of previously published cases, this patient was accepted as a mild variant of syndromic (phenotypic) diarrhea or tricho-hepato-enteric syndrome. We conclude that a mild phenotypic variant of this disease exists that may present with colitis.
引用
收藏
页码:933 / 935
页数:3
相关论文
共 5 条
  • [1] Tricho-hepato-enteric syndrome: A case of hemochromatosis with intractable diarrhea, dysmorphic features, and hair abnormality
    Dweikat, Imad
    Sultan, Mutaz
    Maraqa, Nizar
    Hindi, Tareq
    Abu-Rmeileh, Sara
    Abu-Libdeh, Bassam
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2007, 143A (06) : 581 - 583
  • [2] Intractable diarrhea with "phenotypic anomalies" and tricho-hepato-enteric syndrome:: Two names for the same disorder
    Fabre, Alexandre
    Andre, Nicolas
    Breton, Anne
    Broue, Pierre
    Badens, Catherine
    Roquelaure, Bertrand
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2007, 143A (06) : 584 - 588
  • [3] Syndromic (phenotypic) diarrhea in early infancy
    Goulet, Olivier
    Vinson, Christine
    Roquelaure, Bertrand
    Brousse, Nicole
    Bodemer, Christine
    Cezard, Jean-Pierre
    [J]. ORPHANET JOURNAL OF RARE DISEASES, 2008, 3 (1)
  • [4] Verloes A, 1997, AM J MED GENET, V68, P391, DOI 10.1002/(SICI)1096-8628(19970211)68:4<391::AID-AJMG3>3.0.CO
  • [5] 2-P