메뉴 건너뛰기




Volumn 16, Issue 2, 1996, Pages 173-179

Prenatal ultrasound findings in hydrolethalus: Continuing difficulties in diagnosis

Author keywords

Hydrolethalus; Prenatal diagnosis; Ultrasound

Indexed keywords

ARTICLE; CASE REPORT; FETUS; FETUS MALFORMATION; HUMAN; HYDRAMNIOS; HYDROCEPHALUS; LETHALITY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; ULTRASOUND;

EID: 0030020468     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199602)16:2<173::AID-PD821>3.0.CO;2-I     Document Type: Article
Times cited : (7)

References (23)
  • 1
    • 0021213599 scopus 로고
    • Hydrolethalus syndrome in consecutive African siblings
    • Adetoro, O.O., Komolafe, F., Anjorin, A. (1984). Hydrolethalus syndrome in consecutive African siblings, Pediatr. Radiol., 14, 422-424.
    • (1984) Pediatr. Radiol. , vol.14 , pp. 422-424
    • Adetoro, O.O.1    Komolafe, F.2    Anjorin, A.3
  • 2
    • 0029181736 scopus 로고
    • First-trimester diagnosis of hydrolethalus syndrome
    • Ämmälä, P., Salonen, R. (1995). First-trimester diagnosis of hydrolethalus syndrome, Ultrasound Obstet. Gynecol., 5, 60-62.
    • (1995) Ultrasound Obstet. Gynecol. , vol.5 , pp. 60-62
    • Ämmälä, P.1    Salonen, R.2
  • 9
    • 0026050490 scopus 로고
    • Familial holoprosencephaly, heart defects, and polydactyly
    • Hennekam, R.C.M., Van Noort, G., De La Fuente (1991). Familial holoprosencephaly, heart defects, and polydactyly, Am. J. Med. Genet., 41, 258-262.
    • (1991) Am. J. Med. Genet. , vol.41 , pp. 258-262
    • Hennekam, R.C.M.1    Van Noort, G.2    De La Fuente3
  • 10
    • 0021332903 scopus 로고
    • Roentgenologic findings of the hydrolethalus syndrome
    • Herva, R., Seppänen, U. (1984). Roentgenologic findings of the hydrolethalus syndrome, Pediatr. Radiol., 14, 41-43.
    • (1984) Pediatr. Radiol. , vol.14 , pp. 41-43
    • Herva, R.1    Seppänen, U.2
  • 11
    • 0026009297 scopus 로고
    • Twin fetuses with abnormalities that overlap with three midline malformation complexes
    • Hingorani, S.R., Pagon, R.A., Shepard, T.H., Dapur, R.P. (1991). Twin fetuses with abnormalities that overlap with three midline malformation complexes, Am. J. Med. Genet., 41, 230-235.
    • (1991) Am. J. Med. Genet. , vol.41 , pp. 230-235
    • Hingorani, S.R.1    Pagon, R.A.2    Shepard, T.H.3    Dapur, R.P.4
  • 12
    • 0020615253 scopus 로고
    • The campomelic syndrome: Review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al. in 1971
    • Houston, C.S., Opitz, J.M., Spranger, J.W., Macpherson, R.I., Reed, M.H., Gilbert, E.F., Herrmann, J., Schinzel, A. (1983). The campomelic syndrome: review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al. in 1971, Am. J. Med. Genet., 15, 3-28.
    • (1983) Am. J. Med. Genet. , vol.15 , pp. 3-28
    • Houston, C.S.1    Opitz, J.M.2    Spranger, J.W.3    Macpherson, R.I.4    Reed, M.H.5    Gilbert, E.F.6    Herrmann, J.7    Schinzel, A.8
  • 13
    • 0027270349 scopus 로고
    • Defective cholesterol biosynthesis in Smith-Lemli-Opitz syndrome
    • Letter
    • Irons, M., Elias, E.R., Salen, G., Tint, G.S., Batta, A.K. (1993). Defective cholesterol biosynthesis in Smith-Lemli-Opitz syndrome, Lancet, 341, 1414 (Letter).
    • (1993) Lancet , vol.341 , pp. 1414
    • Irons, M.1    Elias, E.R.2    Salen, G.3    Tint, G.S.4    Batta, A.K.5
  • 14
    • 0001678154 scopus 로고
    • Three dimensional ultrasound in obstetrics and gynecology
    • Kurjac, A., Chervenak, F.A. (Eds). New York: The Parthenon Publishing Group
    • Jurkovic, D., Jauniaux, E., Campbell, S. (1994). Three dimensional ultrasound in obstetrics and gynecology. In: Kurjac, A., Chervenak, F.A. (Eds). The Fetus as a Patient, New York: The Parthenon Publishing Group, 135-140.
    • (1994) The Fetus as a Patient , pp. 135-140
    • Jurkovic, D.1    Jauniaux, E.2    Campbell, S.3
  • 16
    • 0025786027 scopus 로고
    • On lumping and splitting: A fetus with clinical findings of the oral-facial-digital syndrome type VI, the hydrolethalus syndrome, and the Pallister-Hall syndrome
    • Muenke, M., Ruchelli, E.D., Rorke, L.B., McDonald-McGinn, D.M., Orlow, M.K., Isaacs, A., Craparo, F.J., Dunn, L.K., Zackai, E.H. (1991). On lumping and splitting: a fetus with clinical findings of the oral-facial-digital syndrome type VI, the hydrolethalus syndrome, and the Pallister-Hall syndrome, Am. J. Med. Genet., 41, 548-556.
    • (1991) Am. J. Med. Genet. , vol.41 , pp. 548-556
    • Muenke, M.1    Ruchelli, E.D.2    Rorke, L.B.3    McDonald-McGinn, D.M.4    Orlow, M.K.5    Isaacs, A.6    Craparo, F.J.7    Dunn, L.K.8    Zackai, E.H.9
  • 17
    • 0027160513 scopus 로고
    • Two consecutive hydrolethalus syndrome-affected pregnancies in a nonconsanguineous black couple
    • Pryde, P.G., Qureshi, F., Hallak, M., Kupsky, W., Johnson, M., Evans, M. (1993). Two consecutive hydrolethalus syndrome-affected pregnancies in a nonconsanguineous black couple, Am J. Med. Genet., 46, 537-541.
    • (1993) Am J. Med. Genet. , vol.46 , pp. 537-541
    • Pryde, P.G.1    Qureshi, F.2    Hallak, M.3    Kupsky, W.4    Johnson, M.5    Evans, M.6
  • 18
    • 0025198466 scopus 로고
    • Hydrolethalus syndrome
    • Salonen, R., Herva, R. (1990). Hydrolethalus syndrome, J. Med. Genet., 27, 756-759.
    • (1990) J. Med. Genet. , vol.27 , pp. 756-759
    • Salonen, R.1    Herva, R.2
  • 19
    • 0019500186 scopus 로고
    • The hydrolethalus syndrome: Delineation of a 'new', lethal malformation syndrome based on 28 patients
    • Salonen, R., Herva, R., Norio, R. (1981). The hydrolethalus syndrome: delineation of a 'new', lethal malformation syndrome based on 28 patients. Clin. Genet., 19, 321-330.
    • (1981) Clin. Genet. , vol.19 , pp. 321-330
    • Salonen, R.1    Herva, R.2    Norio, R.3
  • 22
    • 0026723476 scopus 로고
    • Variability versus heterogeneity in syndromal hypothalamic hamartoblastoma and related disorders
    • Verloes, A., Gillerot, Y., Langhendries, F.P., Fryns, F.P., Koulischer, L. (1992). Variability versus heterogeneity in syndromal hypothalamic hamartoblastoma and related disorders. Am. J. Med. Genet., 43, 669-677.
    • (1992) Am. J. Med. Genet. , vol.43 , pp. 669-677
    • Verloes, A.1    Gillerot, Y.2    Langhendries, F.P.3    Fryns, F.P.4    Koulischer, L.5
  • 23
    • 0028275502 scopus 로고
    • Meckel syndrome: What are the minimum diagnostic criteria?
    • Wright, C., Healicon, R., English, C., Burn, J. (1994). Meckel syndrome: what are the minimum diagnostic criteria?, J. Med Genet., 31, 482-485.
    • (1994) J. Med Genet. , vol.31 , pp. 482-485
    • Wright, C.1    Healicon, R.2    English, C.3    Burn, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.