Buschke-Ollendorff Syndrome

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منابع مشابه

Buschke-Ollendorff syndrome presenting as a painful nodule

BOS: Buschke-Ollendorff syndrome INTRODUCTION First reported in 1928, Buschke-Ollendorff syndrome (BOS) is an autosomal dominant genodermatosis with high penetrance and variable expressivity. It is characterized by skin-colored or yellow smooth papules, plaques, and nodules up to 2 cm consisting of elastomas or collagenomas, known as dermatofibrosis lenticularis disseminata. This syndrome also ...

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Buschke-Ollendorff syndrome accidentally diagnosed after a left ankle sprain.

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Buschke-Ollendorff syndrome: absence of LEMD3 mutation in an affected family.

BACKGROUND Buschke-Ollendorff syndrome (BOS), an autosomal dominant disorder, features small, acquired, asymptomatic, symmetrical foci of osteosclerosis detected radiographically in epimetaphyseal bone (osteopoikilosis) (OPK) together with connective tissue nevi or juvenile elastomas. Heterozygous, loss-of-function, germline mutation in the LEMD3 gene (which encodes an inner nuclear membrane pr...

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Helen Ollendorff Curth and Curth-Macklin Syndrome

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Helen Ollendorff-Curth: A dermatologist’s lasting legacy

Helen Ollendorff-Curth (Fig. 1) was one of the first female pioneers in academic dermatology and the study of genodermatoses, and her research contributions continue to resonate today. Born in 1899 into a successful Jewish family in Breslau, Germany (now Wroclaw, Poland), she grew up under the guidance of her mother, Paula, a women’s advocate in her own right. Paula was an elected city councilo...

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ژورنال

عنوان ژورنال: Archives of Dermatology

سال: 2010

ISSN: 0003-987X

DOI: 10.1001/archdermatol.2009.320