Benjamin syndrome is a type of multiple congenital anomaly/ intellectual disability (MCA/MR) syndrome. It is characterized by hypochromic anemia with intellectual disability 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 intellectual disability.Jablonski, Stanley (1991).
Jablonski's dictionary of syndromes & eponymic diseases.
' Krieger Pub. Co.

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