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Volumn 12, Issue 2, 2003, Pages 141-142

Solitary median maxillary central incisor, Duane retraction syndrome, growth hormone deficiency and duplicated thumb phalanx: A case report

Author keywords

Duane retraction syndrome; Duplicated thumb phalanx; Growth defect; Holoprosencephaly; Solitary maxillary central incisor; Strabismus

Indexed keywords

ARTICLE; CASE REPORT; CHILD; DISEASE ASSOCIATION; DUANE RETRACTION SYNDROME; GROWTH HORMONE DEFICIENCY; HOLOPROSENCEPHALY; HUMAN; INCISOR; MALE; PRIORITY JOURNAL; STRABISMUS; THUMB MALFORMATION; TOOTH MALFORMATION;

EID: 0038218185     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200304000-00014     Document Type: Article
Times cited : (18)

References (11)
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    • Arlis, H.1    Ward, R.F.2
  • 2
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    • Microphthalmia with single central incisor and hypopituitarism
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    • Artman, H.G.1    Boyden, E.2
  • 3
    • 0000436622 scopus 로고
    • Congenital deficiency of abduction, associated with impairment of abduction, retraction movements, contraction of the palpebral fissure and oblique movements of the eye
    • Duane A (1905). Congenital deficiency of abduction, associated with impairment of abduction, retraction movements, contraction of the palpebral fissure and oblique movements of the eye. Arch Opthalmol 34:133-159.
    • (1905) Arch Opthalmol , vol.34 , pp. 133-159
    • Duane, A.1
  • 5
    • 0022227078 scopus 로고
    • The Okihiro syndrome of Duane anomaly, radial ray abnormalities, and deafness
    • Hayes A, Costa T, Polomeno RC (1985). The Okihiro syndrome of Duane anomaly, radial ray abnormalities, and deafness. Am J Med Genet 22(2):273-280.
    • (1985) Am J Med Genet , vol.22 , Issue.2 , pp. 273-280
    • Hayes, A.1    Costa, T.2    Polomeno, R.C.3
  • 6
    • 0032732443 scopus 로고    scopus 로고
    • The mutational spectrum of the Sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly
    • Nanni L, Ming JE, Bocian M, Steinhaus K, Bianchi DW (1999). The mutational spectrum of the Sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly. Hum Molec Genet 8:2479-2488.
    • (1999) Hum Molec Genet , vol.8 , pp. 2479-2488
    • Nanni, L.1    Ming, J.E.2    Bocian, M.3    Steinhaus, K.4    Bianchi, D.W.5
  • 7
    • 0035934018 scopus 로고    scopus 로고
    • SHH mutation is associated with solitary median maxillary incisor: A study of 13 patients and review of the literature
    • Nanni L, Ming JE, Du Y, Hall RK, Aldred M, Bankier A, Muenke M (2001). SHH mutation is associated with solitary median maxillary incisor: A study of 13 patients and review of the literature. Am J Med Genet 102:1-10.
    • (2001) Am J Med Genet , vol.102 , pp. 1-10
    • Nanni, L.1    Ming, J.E.2    Du, Y.3    Hall, R.K.4    Aldred, M.5    Bankier, A.6    Muenke, M.7
  • 8
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    • Duane syndrome and congenital upper-limb anomalies. A familial occurrence
    • Okihiro MM, Tasaki T, Nakano KK, Bennett BK (1977). Duane syndrome and congenital upper-limb anomalies. A familial occurrence. Arch Neurol 34(3):174-179.
    • (1977) Arch Neurol , vol.34 , Issue.3 , pp. 174-179
    • Okihiro, M.M.1    Tasaki, T.2    Nakano, K.K.3    Bennett, B.K.4
  • 11
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    • Een geval van aandoening van Klippel-Feil gecombineerd met abducensparalyse, retractio bulbi en doofstomheid
    • Wildervanck LS (1952). Een geval van aandoening van Klippel-Feil Gecombineerd met Abducensparalyse, retractio bulbi en Doofstomheid. Ned T Geneesk 96:2752-2755.
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    • Wildervanck, L.S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.