An Iranian family with cutis laxa and classic Ehlers-Danlos syndrome
نویسندگان
چکیده مقاله:
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 characteized 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.
منابع مشابه
Sotos syndrome and cutis laxa.
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متن کاملPRESENTATION OF A PEDIGREE OF AN IRANIAN FAMILY WITH TWO MEMBERS WITH CUTIS LAXA AUTOSOMA LRECESSIVE TYPE I
Congenital cutis laxa is an exceptional condition. No large scale pedigree has been reported from Iran. We report a family with 106 members with two members affected with cutis laxa. Our cases were two patients (male and female) with pre- and postnatal growth retardation, cutis laxa, characteristic facies and other manifestations which proved that they were affected with cutis laxa. Their ...
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عنوان ژورنال
دوره 9 شماره suppl.1
صفحات 10- 10
تاریخ انتشار 2006-12-01
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