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Information Journal Paper

Title

AN IRANIAN FAMILY WITH CUTIS LAXA AND CLASSIC EHLERS-DANLOS SYNDROME

Pages

  49-55

Abstract

 Ehlers-Danlos SYNDROME (EDS) is a heterogenous group of inherited disorders of connective tissue characterized by fragility of the skin and blood vessels, hyperextensibility of the skin and joint hypermobility. CUTIS LAXA is characterized clinically by lax, pendulous skin and histologically by loss of elastic tissue in the dermis. There are some reports of coexistence of CUTIS LAXA with other disorders. We present a case of classic EDS with CUTIS LAXA in an Iranian family.

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    APA: Copy

    MASHAYEKHI GHOUYOUNLOU, V., JAVIDI, Z., TAYEBI MEYBODI, N., FARHOUDI, M., & NAHIDI, Y.. (2006). AN IRANIAN FAMILY WITH CUTIS LAXA AND CLASSIC EHLERS-DANLOS SYNDROME. IRANIAN JOURNAL OF DERMATOLOGY, 9(3 (37 SUPPLEMENT)), 49-55. SID. https://sid.ir/paper/383824/en

    Vancouver: Copy

    MASHAYEKHI GHOUYOUNLOU V., JAVIDI Z., TAYEBI MEYBODI N., FARHOUDI M., NAHIDI Y.. AN IRANIAN FAMILY WITH CUTIS LAXA AND CLASSIC EHLERS-DANLOS SYNDROME. IRANIAN JOURNAL OF DERMATOLOGY[Internet]. 2006;9(3 (37 SUPPLEMENT)):49-55. Available from: https://sid.ir/paper/383824/en

    IEEE: Copy

    V. MASHAYEKHI GHOUYOUNLOU, Z. JAVIDI, N. TAYEBI MEYBODI, M. FARHOUDI, and Y. NAHIDI, “AN IRANIAN FAMILY WITH CUTIS LAXA AND CLASSIC EHLERS-DANLOS SYNDROME,” IRANIAN JOURNAL OF DERMATOLOGY, vol. 9, no. 3 (37 SUPPLEMENT), pp. 49–55, 2006, [Online]. Available: https://sid.ir/paper/383824/en

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