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Jaffe-campanacci syndrome
Saudi Medical Journal. 2005; 26 (1): 104-106
en Inglés | IMEMR | ID: emr-74647
ABSTRACT
This case report describes the clinical, radiological and histopathological features of the Jaffe-Campanacci syndrome as seen in a 6-year-old Qatari male patient who was initially misdiagnosed as a case of systemic neurofibromatosis. Our case has all the diagnostic stigmata of Jaffe-Campanacci syndrome as described in the literature and these include cafe au lait macules, skeletal deformities and multiple histologically confirmed non-ossifying fibromas of the long bones
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Índice: IMEMR (Mediterraneo Oriental) Asunto principal: Síndrome / Neurofibromatosis / Manchas Café con Leche / Diagnóstico Diferencial / Fibroma Límite: Humanos / Masculino Idioma: Inglés Revista: Saudi Med. J. Año: 2005

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Índice: IMEMR (Mediterraneo Oriental) Asunto principal: Síndrome / Neurofibromatosis / Manchas Café con Leche / Diagnóstico Diferencial / Fibroma Límite: Humanos / Masculino Idioma: Inglés Revista: Saudi Med. J. Año: 2005