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Volumn 7, Issue 2, 1998, Pages 79-85

Three patients with the osteochondrodysplasia and hypertrichosis syndrome - Cantu syndrome

Author keywords

Cantu syndrome; Hypertrichosis; Osteochondrodysplasia

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CHILD; CHONDRODYSPLASIA; CLINICAL EXAMINATION; CONGENITAL HEART MALFORMATION; CONSANGUINEOUS MARRIAGE; FEMALE; HUMAN; HYPERTRICHOSIS; MALE; PRIORITY JOURNAL; RIB MALFORMATION; SYNDROME;

EID: 0031919371     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-199804000-00001     Document Type: Article
Times cited : (26)

References (12)
  • 1
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    • A distinct osteochondrodysplasia with hypertrichosis - Individualization of a probable autosomal recessive entity
    • Cantu JM, Garcia-Cruz D, Sanchez-Corona J, Hernandcz A, Nazara Z (1982). A distinct osteochondrodysplasia with hypertrichosis - individualization of a probable autosomal recessive entity. Hum Genet 60:36-41.
    • (1982) Hum Genet , vol.60 , pp. 36-41
    • Cantu, J.M.1    Garcia-Cruz, D.2    Sanchez-Corona, J.3    Hernandcz, A.4    Nazara, Z.5
  • 4
    • 0000547204 scopus 로고
    • Hereditary gingival fibromatosis: Report of an affected family with associated splenomegaly and skeletal and soft tissue abnormalities
    • Laband PF, Habib G, Humphreys GS (1964). Hereditary gingival fibromatosis: report of an affected family with associated splenomegaly and skeletal and soft tissue abnormalities. Oral Surg 17:339-351.
    • (1964) Oral Surg , vol.17 , pp. 339-351
    • Laband, P.F.1    Habib, G.2    Humphreys, G.S.3
  • 5
    • 0028017937 scopus 로고
    • Congentital marked hypertrichosis and Laband Syndrome in a child: Overlap between the gingival fibromatosis-hypertrichosis and Laband Syndromes
    • Lacombe D, Bioilac-Sage P, Sibout M, Daussac E, Lesure F, Manchart JP, Battin J (1994). Congentital marked hypertrichosis and Laband Syndrome in a child: overlap between the gingival fibromatosis-hypertrichosis and Laband Syndromes. Genet Conns 5:251-256.
    • (1994) Genet Conns , vol.5 , pp. 251-256
    • Lacombe, D.1    Bioilac-Sage, P.2    Sibout, M.3    Daussac, E.4    Lesure, F.5    Manchart, J.P.6    Battin, J.7
  • 6
    • 0027291862 scopus 로고
    • Hypertrichosis Universalis Congenital a separate entity, or the same disease as gingival fibromatosis?
    • Lee U, Im SB, Kim D-K (1993). Hypertrichosis Universalis Congenital a separate entity, or the same disease as gingival fibromatosis? Fed Derm 10:263-266.
    • (1993) Fed Derm , vol.10 , pp. 263-266
    • Lee, U.1    Im, S.B.2    Kim, D.-K.3
  • 7
    • 0029856695 scopus 로고    scopus 로고
    • Congenital hypertrichosis, cardiomegaly and mild osteochondrodysplasia
    • Nevin NC, Mulholland HC, Thomas PS (1996). Congenital hypertrichosis, cardiomegaly and mild osteochondrodysplasia. AmJMed Genet 66:33-38.
    • (1996) AmJMed Genet , vol.66 , pp. 33-38
    • Nevin, N.C.1    Mulholland, H.C.2    Thomas, P.S.3
  • 8
    • 0028305583 scopus 로고
    • Reduced renal excretion of uric acid in the Hirsutism-Skeletal Dysplasia-Mental Retardation syndrome
    • Oster O, Wiedemann H-R, Duley IA, Simmonds HA, McBride MB (1994). Reduced renal excretion of uric acid in the Hirsutism-Skeletal Dysplasia-Mental Retardation syndrome. AmJMed Genet 51:165-167.
    • (1994) AmJMed Genet , vol.51 , pp. 165-167
    • Oster, O.1    Wiedemann, H.-R.2    Duley, I.A.3    Simmonds, H.A.4    McBride, M.B.5
  • 9
    • 0014141822 scopus 로고
    • Gingival fibromatosis combined with cherubism
    • Ramon Y, Bermen W, Bubis JJ (1967). Gingival fibromatosis combined with cherubism. Oral Surgery 24:436-440.
    • (1967) Oral Surgery , vol.24 , pp. 436-440
    • Ramon, Y.1    Bermen, W.2    Bubis, J.J.3
  • 10
    • 0000964284 scopus 로고
    • Syndrome of gingival hyperplasia, hirsutism and convulsions
    • Snyder CH (1965). Syndrome of gingival hyperplasia, hirsutism and convulsions. J Pediatr 67:499-502.
    • (1965) J Pediatr , vol.67 , pp. 499-502
    • Snyder, C.H.1
  • 11
    • 0027212896 scopus 로고
    • Hirsutism-Skeletal Dysplasia-Mental Retardation Syndrome with abnormal face and a uric acid metabolism disorder
    • Wiedemann H-R, Oldigs H-D, Oppermann H-C, Oster O (1993). Hirsutism-Skeletal Dysplasia-Mental Retardation Syndrome with abnormal face and a uric acid metabolism disorder. AmJMed Genet 46:403-409.
    • (1993) AmJMed Genet , vol.46 , pp. 403-409
    • Wiedemann, H.-R.1    Oldigs, H.-D.2    Oppermann, H.-C.3    Oster, O.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.