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Volumn 16, Issue 8, 2010, Pages 6-

CHILD syndrome with thrombocytosis and congenital dislocation of hip: A case report from India

Author keywords

[No Author keywords available]

Indexed keywords

ANONYCHIA; ARTICLE; CASE REPORT; CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM NEVUS AND LIMB DEFECT; CONGENITAL HIP DISLOCATION; CONSERVATIVE TREATMENT; DISEASE ASSOCIATION; FEMALE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; INDIAN; INFANT; INFLAMMATORY INFILTRATE; LABORATORY DIAGNOSIS; LEG LENGTH INEQUALITY; LEUKOPOIESIS; NAIL DYSTROPHY; NEUTROPHIL GRANULE; NEWBORN; PARAKERATOSIS; PNEUMONIA; SKIN DEFECT; SKIN EXAMINATION; SKIN HYPERTROPHY; SYSTEMIC DISEASE; THORAX RADIOGRAPHY; THROMBOCYTOSIS;

EID: 77958147533     PISSN: None     EISSN: 10872108     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (9)

References (12)
  • 1
    • 22544483962 scopus 로고    scopus 로고
    • Naevi and other developmental defects
    • In: Burns T, Breathnach S, and Cox N, Ed, 7th ed. Oxford: Blackwell Science
    • Atherton DJ, Moss C. Naevi and other developmental defects. In: Burns T, Breathnach S, and Cox N, Ed. Rook's Textbook of Dermatology, 7th ed. Oxford: Blackwell Science; 2004: 15.1-15.114
    • (2004) Rook's Textbook of Dermatology
    • Atherton, D.J.1    Moss, C.2
  • 3
    • 0025038684 scopus 로고
    • Ptychotropism as a cutaneous feature of the CHILD syndrome
    • Happle R. Ptychotropism as a cutaneous feature of the CHILD syndrome. J Am Acad Dermatol. 1990; 23(4): 763-766.
    • (1990) J Am Acad Dermatol , vol.23 , Issue.4 , pp. 763-766
    • Happle, R.1
  • 4
    • 0015068862 scopus 로고
    • Syndrome of unilateral ectromelia, psoriasis and central nervous system anomalies
    • Shear CS, Nyhan WL, Frost P, Weinstein GO. Syndrome of unilateral ectromelia, psoriasis and central nervous system anomalies. Birth Defects. 1971; 7(8):197-203.
    • (1971) Birth Defects , vol.7 , Issue.8 , pp. 197-203
    • Shear, C.S.1    Nyhan, W.L.2    Frost, P.3    Weinstein, G.O.4
  • 5
    • 0021252705 scopus 로고
    • The CHILD syndrome - congenital hemidysplasia with icthyosiform erythroderma & Limb Defects
    • Christiansen JV, Overgaard Petersen H, Søgaard H. The CHILD syndrome - congenital hemidysplasia with icthyosiform erythroderma & Limb Defects. Acta Derm Venereol. 1984; 64:165-168.
    • (1984) Acta Derm Venereol , vol.64 , pp. 165-168
    • Christiansen, J.V.1    Overgaard Petersen, H.2    Søgaard, H.3
  • 6
    • 0012935299 scopus 로고    scopus 로고
    • Left-sided CHILD syndrome caused by a nonsense mutation in the NSDHL gene
    • Hummel M, Cunningham D, Mullett CJ, Kelley RI, Herman GE. Left-sided CHILD syndrome caused by a nonsense mutation in the NSDHL gene. Am J Med Genet. 2003; 122A (3):246-51.
    • (2003) Am J Med Genet , vol.122 A , Issue.3 , pp. 246-251
    • Hummel, M.1    Cunningham, D.2    Mullett, C.J.3    Kelley, R.I.4    Herman, G.E.5
  • 7
    • 54249116888 scopus 로고    scopus 로고
    • A novel silent mutation in the NSDHL gene causing CHILD syndrome as a result of aberrant splicing
    • Saito M, Ishiko A. A novel silent mutation in the NSDHL gene causing CHILD syndrome as a result of aberrant splicing. Br J Dermatol. 2008; 159(5):1204-6.
    • (2008) Br J Dermatol , vol.159 , Issue.5 , pp. 1204-1206
    • Saito, M.1    Ishiko, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.