메뉴 건너뛰기




Volumn 126 A, Issue 4, 2004, Pages 427-429

Two New Cases of Barraquer-Simons Syndrome

Author keywords

Barraquer Simons syndrome; Cephalothoracic lipodystrophy; Partial lipodystrophy

Indexed keywords

ARTICLE; BARRAQUER SIMONS SYNDROME; CASE REPORT; CHILD; CLINICAL FEATURE; COMORBIDITY; DISEASE ASSOCIATION; DISEASE COURSE; FACE MALFORMATION; FEMALE; HUMAN; LIPODYSTROPHY; PRIORITY JOURNAL; SUBCUTANEOUS FAT DISORDER; SUBCUTANEOUS TISSUE; SYNDROME;

EID: 2142647268     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.20623     Document Type: Article
Times cited : (9)

References (14)
  • 1
    • 0018102725 scopus 로고
    • Cephalothoracic lipodystrophy with hypocomplementemic renal disease: Discordance in identical twin sisters
    • Bier DM, O'Connell JJ, Kaplan SL. 1978. Cephalothoracic lipodystrophy with hypocomplementemic renal disease: Discordance in identical twin sisters. J Clin Endocrinol Metab 46:800-807.
    • (1978) J Clin Endocrinol Metab , vol.46 , pp. 800-807
    • Bier, D.M.1    O'Connell, J.J.2    Kaplan, S.L.3
  • 2
    • 0034165815 scopus 로고    scopus 로고
    • Barraquer-Simons sindrome. Report of a case and review of the literature
    • Branisteanu DD, Zbranca E. 2000. Barraquer-Simons sindrome. Report of a case and review of the literature. Rev Med Chir Soc Med Nat Iasi 104:155-158.
    • (2000) Rev Med Chir Soc Med Nat Iasi , vol.104 , pp. 155-158
    • Branisteanu, D.D.1    Zbranca, E.2
  • 3
    • 0033810092 scopus 로고    scopus 로고
    • Renal transplantation in a patient with Barraquer-Simons disease and mesangiocapillary glomerulonephritis type II
    • Chopra S, Isaac R, Mammen K, Pawar B. 2000. Renal transplantation in a patient with Barraquer-Simons disease and mesangiocapillary glomerulonephritis type II. Nephrol Dial Transplant 15:1723-1724.
    • (2000) Nephrol Dial Transplant , vol.15 , pp. 1723-1724
    • Chopra, S.1    Isaac, R.2    Mammen, K.3    Pawar, B.4
  • 6
    • 0022593193 scopus 로고
    • Familial partial lipodystrophy: Two types of an X linked dominant syndrome, lethal in the hemizygous state
    • Kobberling J, Dunningan MG. 1986. Familial partial lipodystrophy: Two types of an X linked dominant syndrome, lethal in the hemizygous state. J Med Genet 23:120-127.
    • (1986) J Med Genet , vol.23 , pp. 120-127
    • Kobberling, J.1    Dunningan, M.G.2
  • 7
    • 33646208100 scopus 로고
    • Partial lipodystrophy ("facies Voltarien") and hypocomplementaemic nephritis
    • Kraai EJ, van Son W. 1983. Partial lipodystrophy ("facies Voltarien") and hypocomplementaemic nephritis. Br J Dermatol 108:115-116.
    • (1983) Br J Dermatol , vol.108 , pp. 115-116
    • Kraai, E.J.1    Van Son, W.2
  • 8
    • 0040739918 scopus 로고
    • Zur Lypodystrophia progressiva
    • Langhof H, Zabel R. 1960. Zur Lypodystrophia progressiva. Arch Klin Exp Derm 210:313-321.
    • (1960) Arch Klin Exp Derm , vol.210 , pp. 313-321
    • Langhof, H.1    Zabel, R.2
  • 9
    • 0014485439 scopus 로고
    • Familial epilepsy and progressive partial lipodystrophy (Barraquer-Simons disease)
    • Laxenaire M, Weber M, Tridon P. 1969. Familial epilepsy and progressive partial lipodystrophy (Barraquer-Simons disease). Epilepsia 10:87-90.
    • (1969) Epilepsia , vol.10 , pp. 87-90
    • Laxenaire, M.1    Weber, M.2    Tridon, P.3
  • 10
    • 0019932136 scopus 로고
    • Multifocal interstitial myositis associated with localized lipoatrophy: A benign course
    • Palliyath S, Garcia CA. 1982. Multifocal interstitial myositis associated with localized lipoatrophy: A benign course. Arch Neurol 39:722.
    • (1982) Arch Neurol , vol.39 , pp. 722
    • Palliyath, S.1    Garcia, C.A.2
  • 13
    • 0016900516 scopus 로고
    • Membranoproliferative glomerulonephritis with partial lipodystrophy: Discordant occurrence in identical twins
    • Reichel W, Kobberling J, Fischbach H, Scheler F. 1976. Membranoproliferative glomerulonephritis with partial lipodystrophy: Discordant occurrence in identical twins. Klin Wochenschr 54:75-81.
    • (1976) Klin Wochenschr , vol.54 , pp. 75-81
    • Reichel, W.1    Kobberling, J.2    Fischbach, H.3    Scheler, F.4
  • 14
    • 0030756662 scopus 로고    scopus 로고
    • Barraquer-Simons syndrome (with sensorineural deafness): A contribution to the differential diagnosis of lipodystrophy syndromes
    • Spranger S, Spranger M, Tasman AJ, Reith W, Voigtlander V. 1997. Barraquer-Simons syndrome (with sensorineural deafness): A contribution to the differential diagnosis of lipodystrophy syndromes. Am J Med Genet 71:397-400.
    • (1997) Am J Med Genet , vol.71 , pp. 397-400
    • Spranger, S.1    Spranger, M.2    Tasman, A.J.3    Reith, W.4    Voigtlander, V.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.