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Volumn 50, Issue 2 SUPPL., 2004, Pages

Progressive multilayered banded skin in Winchester syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ACNE; ADULT; AGE DISTRIBUTION; ARTICLE; BONE INJURY; BONE MALFORMATION; CARPAL BONE; CASE REPORT; CLINICAL FEATURE; COARSE FACE; CORNEA OPACITY; FEMALE; FUNCTIONAL DISEASE; GENETIC DISORDER; GENETIC HETEROGENEITY; GINGIVA HYPERTROPHY; GRANULOMA ANNULARE; HUMAN; HYPERPIGMENTATION; HYPERTRICHOSIS; INHERITANCE; JOINT CONTRACTURE; LEATHERY SKIN; OSTEOLYSIS; OSTEOPOROSIS; PHENOTYPE; PRIORITY JOURNAL; SHORT STATURE; SKIN DISEASE; SUBCUTANEOUS NODULE; SYNDROME DELINEATION; TARSAL BONE; THICKNESS; WINCHESTER SYNDROME;

EID: 0842347484     PISSN: 01909622     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0190-9622(03)02466-6     Document Type: Article
Times cited : (18)

References (15)
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    • Lachman, R.S.1
  • 9
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    • New form of idiopathic osteolysis: Nodulosis, Arthropathy and Osteolysis (NAO) syndrome
    • Al-Mayouf SM, Majeed M, Hugosson C, Bahabri S. New form of idiopathic osteolysis: Nodulosis, Arthropathy and Osteolysis (NAO) syndrome. Am J Med Genet 2000;93:5-10.
    • (2000) Am J Med Genet , vol.93 , pp. 5-10
    • Al-Mayouf, S.M.1    Majeed, M.2    Hugosson, C.3    Bahabri, S.4
  • 11
    • 0024326891 scopus 로고
    • Syndrome of the month: Winchester's syndrome
    • Winter RM. Syndrome of the month: Winchester's syndrome. J Med Genet 1989;26:772-5.
    • (1989) J Med Genet , vol.26 , pp. 772-775
    • Winter, R.M.1
  • 12
    • 0014806192 scopus 로고
    • Peripheral corneal opacification and skeletal deformities: A newly recognised acid mucopolysaccharidosis simulating rheumatoid arthritis
    • Brown SI, Kuwabara T. Peripheral corneal opacification and skeletal deformities: A newly recognised acid mucopolysaccharidosis simulating rheumatoid arthritis. Arch Ophthalmol 1970;83:667-77.
    • (1970) Arch Ophthalmol , vol.83 , pp. 667-677
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  • 14
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    • Mutation of the matrix metalloproteinase 2 gene (MMP2) causes a multicentric osteolysis and arthritis syndrome
    • Martignetti JA, Al Aqeel A, Al Sewairi W, Boumah CE, Kambouris M, Al Mayouf S, et al. Mutation of the matrix metalloproteinase 2 gene (MMP2) causes a multicentric osteolysis and arthritis syndrome. Nat Genet 2001;28:261-5.
    • (2001) Nat Genet , vol.28 , pp. 261-265
    • Martignetti, J.A.1    Al Aqeel, A.2    Al Sewairi, W.3    Boumah, C.E.4    Kambouris, M.5    Al Mayouf, S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.