LEOPARD syndrome with rare skeletal anomalies: A case report
نویسندگان
چکیده
منابع مشابه
LEOPARD syndrome: Report of a case
LEOPARD syndrome is an autosomal dominant hereditary disease, which is characterized with cutaneous pigmented patches, electrocardiographic changes, ocular hypertelorism, retarded growth, pulmonic stenosis, genital abnormalities and congenital deafness. The gene of this disease have high penetrance but expression is varied and incomplete forms may be seen. We report a 23 year-old woman wi...
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A 40-year-old man presented with palpitation for 2 days. His past medical history was unremarkable. Physical examination revealed that multiple lentigines of 5 mm to 15 mm that were black-brown in color, macule, flat, and scattered on the face, neck, trunk, and on both hands (Fig. 1A). Hypertelorism was found but there were no evidences of deafness, genital anomaly, and other dysmorphic feature...
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ژورنال
عنوان ژورنال: Indian Journal of Dermatology
سال: 2013
ISSN: 0019-5154
DOI: 10.4103/0019-5154.117362