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Benjamin syndrome : ウィキペディア英語版 | Benjamin syndrome
Benjamin Syndrome (or Benjamin anemia) is a type of multiple congenital anomaly/mental retardation (MCA/MR) syndrome. It is characterized by hypochromic anemia with mental deficiency and various craniofacial and other anomalies. It can also include heart murmur, dental caries and splenic tumors. It was first described in the medical literature in 1911.〔Benjamin E (1911). Über eine selbständige Form der Anämie im frühen Kindersalter. ''Verh Deut Ges Kinderh'', 1911,119-24.〕 Symptoms include megalocephaly, external ear deformities, dental caries, micromelia, hypoplastic bone deformities, hypogonadism, hypochromic anemia with occasional tumors, and mental retardation.〔Jablonski, Stanley (1991). ''(Jablonski's dictionary of syndromes & eponymic diseases. )'' Krieger Pub. Co. ISBN 978-0-89464-224-1〕 ==References==
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