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Journal Abstract Search

165 related items for PubMed ID: 20886807

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  • 2. A novel X-chromosomal microdeletion encompassing congenital hemidysplasia with ichthyosiform erythroderma and limb defects.
    Raychaudhury T, George R, Mandal K, Srivastava VM, Thomas M, Bornholdt D, Grzeschik KH, Koehler A.
    Pediatr Dermatol; 2013; 30(2):250-2. PubMed ID: 22471832
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  • 5. CHILD syndrome mimicking verrucous nevus in a Chinese patient responded well to the topical therapy of compound of simvastatin and cholesterol.
    Yu X, Zhang J, Gu Y, Deng D, Wu Z, Bao L, Li M, Yao Z.
    J Eur Acad Dermatol Venereol; 2018 Jul; 32(7):1209-1213. PubMed ID: 29341259
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  • 9. CHILD syndrome: effective treatment of ichthyosiform naevus with oral and topical ketoconazole.
    Liu T, Qian G, Wang XX, Zhang YG.
    Acta Derm Venereol; 2015 Jan; 95(1):91-2. PubMed ID: 24696032
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  • 10. Late evolution of giant verruciform xanthoma in the setting of CHILD syndrome.
    Kurban M, Abbas O, Ghosn S, Kibbi AG.
    Pediatr Dermatol; 2010 Jan; 27(5):551-3. PubMed ID: 20796237
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  • 11. Verrucous hyperkeratosis with predominant involvement of the left side of the body and concomitant onychodystrophy in a 17-year-old girl.
    Armina S, Heiko T, Rudolf H, Judith F, Dimitra K, Peter S.
    J Dtsch Dermatol Ges; 2020 Sep; 18(9):1054-1057. PubMed ID: 32515052
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  • 12. CHILD syndrome caused by a deletion of exons 6-8 of the NSDHL gene.
    Kim CA, Konig A, Bertola DR, Albano LM, Gattás GJ, Bornholdt D, Leveleki L, Happle R, Grzeschik KH.
    Dermatology; 2005 Sep; 211(2):155-8. PubMed ID: 16088165
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  • 13. CHILD syndrome with thrombocytosis and congenital dislocation of hip: A case report from India.
    Chander R, Varghese B, Jabeen M, Garg T, Jain M.
    Dermatol Online J; 2010 Aug 15; 16(8):6. PubMed ID: 20804683
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  • 14. Congenital hemidysplasia with ichthyosiform naevus and limb defects (CHILD) syndrome without hemidysplasia.
    Estapé A, Josifova D, Rampling D, Glover M, Kinsler VA.
    Br J Dermatol; 2015 Jul 15; 173(1):304-7. PubMed ID: 25533639
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  • 16. CHILD syndrome: A modified pathogenesis-targeted therapeutic approach.
    Bergqvist C, Abdallah B, Hasbani DJ, Abbas O, Kibbi AG, Hamie L, Kurban M, Rubeiz N.
    Am J Med Genet A; 2018 Mar 15; 176(3):733-738. PubMed ID: 29392821
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  • 17. Novel NSDHL gene variant for congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD) syndrome.
    Maceda EBG, Kratz LE, Ramos VME, Abacan MAR.
    BMJ Case Rep; 2020 Nov 02; 13(11):. PubMed ID: 33139364
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  • 19. The role of abnormalities in the distal pathway of cholesterol synthesis in the Congenital Hemidysplasia with Ichthyosiform erythroderma and Limb Defects (CHILD) syndrome.
    Seeger MA, Paller AS.
    Biochim Biophys Acta; 2014 Mar 02; 1841(3):345-52. PubMed ID: 24060582
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