메뉴 건너뛰기




Volumn 35, Issue 3, 2008, Pages 156-160

Lowe syndrome: Literature review and case report

Author keywords

Low syndrome; Orthodontic treatment

Indexed keywords

ADOLESCENT; ARTICLE; CANINE TOOTH; CASE REPORT; CEPHALOMETRY; CONGENITAL MALFORMATION; DECIDUOUS TOOTH; HUMAN; LOWE SYNDROME; MALE; MALOCCLUSION; MOLAR TOOTH; PANORAMIC RADIOGRAPHY; PATHOLOGY; PATHOPHYSIOLOGY; PHYSIOLOGY; TOOTH DISEASE; TOOTH ERUPTION; TOOTH PULP;

EID: 54049156569     PISSN: 14653125     EISSN: None     Source Type: Journal    
DOI: 10.1179/146531207225022599     Document Type: Article
Times cited : (10)

References (15)
  • 1
    • 0000623605 scopus 로고
    • Organic-aciduria, decreased renal ammonia production, hydrophthalmos, and mental retardation; a clinical entity
    • Lowe CU, Terrey M, MacLachlan EA. Organic-aciduria, decreased renal ammonia production, hydrophthalmos, and mental retardation; a clinical entity. AMA Am J Dis Child 1952; 83: 164-84.
    • (1952) AMA Am J Dis Child , vol.83 , pp. 164-184
    • Lowe, C.U.1    Terrey, M.2    MacLachlan, E.A.3
  • 2
    • 0023320251 scopus 로고
    • Update: Lowe's syndrome
    • Wappner RS. Update: Lowe's syndrome. Compr Ther 1987; 13: 3-4.
    • (1987) Compr Ther , vol.13 , pp. 3-4
    • Wappner, R.S.1
  • 4
    • 0030971762 scopus 로고    scopus 로고
    • Spectrum of mutations in the OCRL1 gene in the Lowe oculocerebrorenal syndrome
    • Lin T, Orrison BM, Leahey AM, et al. Spectrum of mutations in the OCRL1 gene in the Lowe oculocerebrorenal syndrome. Am J Hum Genet 1997; 60: 1384-88.
    • (1997) Am J Hum Genet , vol.60 , pp. 1384-1388
    • Lin, T.1    Orrison, B.M.2    Leahey, A.M.3
  • 5
    • 0032072943 scopus 로고    scopus 로고
    • Mutations are not uniformly distributed throughout the OCRL1 gene in Lowe syndrome patients
    • Lin T, Orrison BM, Leahey AM, et al. Mutations are not uniformly distributed throughout the OCRL1 gene in Lowe syndrome patients. Mol Genet Metab 1998; 64: 58-61.
    • (1998) Mol Genet Metab , vol.64 , pp. 58-61
    • Lin, T.1    Orrison, B.M.2    Leahey, A.M.3
  • 6
    • 0029060795 scopus 로고
    • The protein deficient in Lowe syndrome is a phosphatidylinositol-4,5-bisphosphate 5-phosphatase
    • Zhang X, Jefferson AB, Auethavekiat V, Majerus PW. The protein deficient in Lowe syndrome is a phosphatidylinositol-4,5-bisphosphate 5-phosphatase. Proc Nat Acad Sci USA 1995; 92: 4853-56.
    • (1995) Proc Nat Acad Sci USA , vol.92 , pp. 4853-4856
    • Zhang, X.1    Jefferson, A.B.2    Auethavekiat, V.3    Majerus, P.W.4
  • 7
    • 0028880052 scopus 로고
    • Lowe syndrome, a deficiency of phosphatidylinositol 4,5-bisphosphate 5-phosphatase in the Golgi apparatus
    • Suchy SF, Olivos-Glander IM, Nussabaum RL. Lowe syndrome, a deficiency of phosphatidylinositol 4,5-bisphosphate 5-phosphatase in the Golgi apparatus. Hum Mol Genet 1995; 4: 2245-50.
    • (1995) Hum Mol Genet , vol.4 , pp. 2245-2250
    • Suchy, S.F.1    Olivos-Glander, I.M.2    Nussabaum, R.L.3
  • 10
    • 0022628074 scopus 로고
    • Orthopedic manifestations of the Lowe (oculocerebrorenal) syndrome
    • Holtgrewe JL, Kalen V. Orthopedic manifestations of the Lowe (oculocerebrorenal) syndrome. J Pediatr Orthop 1986; 6: 165-71.
    • (1986) J Pediatr Orthop , vol.6 , pp. 165-171
    • Holtgrewe, J.L.1    Kalen, V.2
  • 11
    • 0028186416 scopus 로고
    • Lowe's syndrome: Review of literature and report of case
    • Thomas GP, Grimm SE. Lowe's syndrome: review of literature and report of case. ASDC J Dent Child 1994; 61: 68-70.
    • (1994) ASDC J Dent Child , vol.61 , pp. 68-70
    • Thomas, G.P.1    Grimm, S.E.2
  • 15
    • 0034684719 scopus 로고    scopus 로고
    • Unusual renal features of Lowe syndrome in a mildly affected boy
    • Gropman A, Levin S, Yao L, et al. Unusual renal features of Lowe syndrome in a mildly affected boy. Am J Med Genet 2000; 95: 461-66.
    • (2000) Am J Med Genet , vol.95 , pp. 461-466
    • Gropman, A.1    Levin, S.2    Yao, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.