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Volumn 14, Issue 3, 2005, Pages 155-158

Growth deficiency in oculodigitoesophagoduodenal (Feingold) syndrome - Case report and review of the literature

Author keywords

Feingold; Growth deficiency

Indexed keywords

CLONIDINE;

EID: 21244448003     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200507000-00011     Document Type: Review
Times cited : (5)

References (16)
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    • Brunner HG, Winter RM (1991). Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresia. J Med Genet 28:389-394.
    • (1991) J Med Genet , vol.28 , pp. 389-394
    • Brunner, H.G.1    Winter, R.M.2
  • 4
    • 0141993865 scopus 로고    scopus 로고
    • Feingold syndrome: Clinical review and genetic mapping
    • Celli J, van Bokhoven H, Brunner HG (2003). Feingold syndrome: clinical review and genetic mapping. Am J Med Genet 122:294-300.
    • (2003) Am J Med Genet , vol.122 , pp. 294-300
    • Celli, J.1    Van Bokhoven, H.2    Brunner, H.G.3
  • 6
    • 0032722486 scopus 로고    scopus 로고
    • Feingold syndrome - A cause of profound deafness
    • Dodds A, Ramsden R, Kingston H (1999). Feingold syndrome - a cause of profound deafness. J Laryngol Otol 10:919-921.
    • (1999) J Laryngol Otol , vol.10 , pp. 919-921
    • Dodds, A.1    Ramsden, R.2    Kingston, H.3
  • 7
    • 0003593937 scopus 로고
    • Case report 30
    • Feingold M (1975). Case report 30. Synd Ident 3:16-17.
    • (1975) Synd Ident , vol.3 , pp. 16-17
    • Feingold, M.1
  • 8
    • 0031002838 scopus 로고    scopus 로고
    • Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay
    • Feingold M, Hall BD, Lacassie Y, Martinez-Frias ML (1997). Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay. Am J Med Genet 69:245-249.
    • (1997) Am J Med Genet , vol.69 , pp. 245-249
    • Feingold, M.1    Hall, B.D.2    Lacassie, Y.3    Martinez-Frias, M.L.4
  • 10
    • 4544220256 scopus 로고    scopus 로고
    • Feingold syndrome: Microcephaly, esophageal atresia, type III laryngeal cleft, malrotation, limb anomalies
    • Herman TE, Siegel MJ (2004). Feingold syndrome: microcephaly, esophageal atresia, type III laryngeal cleft, malrotation, limb anomalies. J Perinatol 9: 568-570.
    • (2004) J Perinatol , vol.9 , pp. 568-570
    • Herman, T.E.1    Siegel, M.J.2
  • 12
    • 0030738131 scopus 로고    scopus 로고
    • Autosomal dominant microcephaly with normal intelligence, short palpebral fissures, and digital anomalies
    • Innis JW, Asher JH Jr, Poznanski AK, Sheldon S (1997). Autosomal dominant microcephaly with normal intelligence, short palpebral fissures, and digital anomalies. Am J Med Genet 71:150-155.
    • (1997) Am J Med Genet , vol.71 , pp. 150-155
    • Innis, J.W.1    Asher Jr., J.H.2    Poznanski, A.K.3    Sheldon, S.4
  • 13
    • 0030959498 scopus 로고    scopus 로고
    • Digital anomalies, microcephaly, and normal intelligence: New syndrome or Feingold syndrome?
    • Kawame H, Pagon RA, Hudgins L (1997). Digital anomalies, microcephaly, and normal intelligence: new syndrome or Feingold syndrome? Am J Med Genet 69:240-244.
    • (1997) Am J Med Genet , vol.69 , pp. 240-244
    • Kawame, H.1    Pagon, R.A.2    Hudgins, L.3
  • 14
    • 0025042565 scopus 로고
    • Microcephaly, mesobrachyphalangy, and tracheo-oesophageal fistula: MMT syndrome
    • Konig R, Selzer G, Stolp A, Fuchs S (1990). Microcephaly, mesobrachyphalangy, and tracheo-oesophageal fistula: MMT syndrome. Dysmorph Clin Genet 4:83-86.
    • (1990) Dysmorph Clin Genet , vol.4 , pp. 83-86
    • Konig, R.1    Selzer, G.2    Stolp, A.3    Fuchs, S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.