메뉴 건너뛰기




Volumn 13, Issue 4, 2004, Pages 247-250

Hypertrichosis, fallot tetralogy, growth and developmental delay

Author keywords

Developmental delay; Fallot tetralogy; Hypertrichosis

Indexed keywords

CYCLOSPORIN; DIAZOXIDE; DIGOXIN; TOPIRAMATE; VALPROIC ACID;

EID: 16644379524     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200410000-00009     Document Type: Article
Times cited : (6)

References (14)
  • 1
    • 0024312174 scopus 로고
    • Idiopathic familial gingival fibromatosis associated with mental retardation, epilepsy and hypertrichosis
    • Anavi Y, Lerman P, Mintz S, Kiviti S (1989). Idiopathic familial gingival fibromatosis associated with mental retardation, epilepsy and hypertrichosis. Dev Med Child Neurol 31:538-542.
    • (1989) Dev Med Child Neurol , vol.31 , pp. 538-542
    • Anavi, Y.1    Lerman, P.2    Mintz, S.3    Kiviti, S.4
  • 2
    • 0027504043 scopus 로고
    • Ambras syndrome: Delineation of a unique hypertrichosis universalis congenita and association with a balanced pericentric inversion (8) (p11.2; q22)
    • Baumeister FA, Egger J, Schildhauer MT, Stengel-Rutkowski S (1993). Ambras syndrome: delineation of a unique hypertrichosis universalis congenita and association with a balanced pericentric inversion (8) (p11.2; q22). Clin Genet 44(3):121-128.
    • (1993) Clin Genet , vol.44 , Issue.3 , pp. 121-128
    • Baumeister, F.A.1    Egger, J.2    Schildhauer, M.T.3    Stengel-Rutkowski, S.4
  • 4
    • 0028471874 scopus 로고    scopus 로고
    • Laband syndrome: Report of two cases, review of the literature, and identification of additional manifestations
    • Chadwick B, Hunter B, Hunter L, Aldred M, Wilkie A (1998). Laband syndrome: report of two cases, review of the literature, and identification of additional manifestations. Oral Surg Oral Med Oral Path Oral Radiol 78:57-63.
    • (1998) Oral Surg Oral Med Oral Path Oral Radiol , vol.78 , pp. 57-63
    • Chadwick, B.1    Hunter, B.2    Hunter, L.3    Aldred, M.4    Wilkie, A.5
  • 6
    • 0034722844 scopus 로고    scopus 로고
    • Syndrome of gingival hypertrophy, hirsutism, mental retardation and brachymetacarpia in two sisters: Specific entity or variant of a described condition?
    • Gohlich-Ratmann G, Lackner A, Schaper J, Voit T, Gillessen-Kaesbach G (2000). Syndrome of gingival hypertrophy, hirsutism, mental retardation and brachymetacarpia in two sisters: specific entity or variant of a described condition? Am J Med Genet 95:241-246.
    • (2000) Am J Med Genet , vol.95 , pp. 241-246
    • Gohlich-Ratmann, G.1    Lackner, A.2    Schaper, J.3    Voit, T.4    Gillessen-Kaesbach, G.5
  • 8
    • 0029808815 scopus 로고    scopus 로고
    • An autosomal dominant syndrome of acromegaloid facial appearance and generalised hypertrichosis terminalis
    • Irvine AD, Dolan OM, Hadden DR, Stewart FJ, Bingham EA, Nevin NC (1996). An autosomal dominant syndrome of acromegaloid facial appearance and generalised hypertrichosis terminalis. J Med Genet 33:972-974.
    • (1996) J Med Genet , vol.33 , pp. 972-974
    • Irvine, A.D.1    Dolan, O.M.2    Hadden, D.R.3    Stewart, F.J.4    Bingham, E.A.5    Nevin, N.C.6
  • 9
    • 0024383996 scopus 로고
    • Cone-rod congenital amaurosis associated with congenital hypertrichosis: An autosomal recessive condition
    • Jalili IK (1989). Cone-rod congenital amaurosis associated with congenital hypertrichosis: an autosomal recessive condition. J Med Genet 26:504-510.
    • (1989) J Med Genet , vol.26 , pp. 504-510
    • Jalili, I.K.1
  • 11
    • 0042824228 scopus 로고    scopus 로고
    • Very long eyelashes, long eyebrows, sparse hair, and mental retardation in two unrelated boys: An atypical form of Oliver-McFarlane syndrome without retinal degeneration, or a new clinical entity?
    • Kondoh T, Amamoto N, Hirota T, Kinoshita E, Moriuchi H, Matsumoto T, Shimono M, Kawakami A, Shirahata A (2003). Very long eyelashes, long eyebrows, sparse hair, and mental retardation in two unrelated boys: an atypical form of Oliver-McFarlane syndrome without retinal degeneration, or a new clinical entity? Am J Med Genet 120A:437-438.
    • (2003) Am J Med Genet , vol.120 A , pp. 437-438
    • Kondoh, T.1    Amamoto, N.2    Hirota, T.3    Kinoshita, E.4    Moriuchi, H.5    Matsumoto, T.6    Shimono, M.7    Kawakami, A.8    Shirahata, A.9
  • 12
    • 0027220991 scopus 로고
    • Hypertrichosis, atrophic skin, ectropion, and macrostomia (Barber-Say syndrome): Report of a new case
    • Martinez Santana S, Perez Alvarez F, Frias JL, Martinez-Frias ML (1993). Hypertrichosis, atrophic skin, ectropion, and macrostomia (Barber-Say syndrome): report of a new case. Am J Med Genet 47:20-23.
    • (1993) Am J Med Genet , vol.47 , pp. 20-23
    • Martinez Santana, S.1    Perez Alvarez, F.2    Frias, J.L.3    Martinez-Frias, M.L.4
  • 13
    • 0000914496 scopus 로고
    • Congenital trichomegaly with associated pigmentary degeneration of the retina, dwarfism and mental retardation
    • Oliver GL, McFarlane DC (1965). Congenital trichomegaly with associated pigmentary degeneration of the retina, dwarfism and mental retardation. Arch Ophthal 74:169-171.
    • (1965) Arch Ophthal , vol.74 , pp. 169-171
    • Oliver, G.L.1    McFarlane, D.C.2
  • 14
    • 0034940079 scopus 로고    scopus 로고
    • Primary generalized and localized hypertrichosis in children
    • Vashi RA, Mancini AJ, Paller AS (2001). Primary generalized and localized hypertrichosis in children. Arch Dermatol 137:877-884.
    • (2001) Arch Dermatol , vol.137 , pp. 877-884
    • Vashi, R.A.1    Mancini, A.J.2    Paller, A.S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.